Gene neighbors for Gene (Select 84677) - Gene - NCBI

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Name/Gene ID	Description	Location	Aliases	MIM
Select item 129664727 LOC129664727 ID: 129664727	ReSE screen-validated silencer GRCh37_chr21:39261680-39261872 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (37889377..37889569)
Select item 127894658 LOC127894658 ID: 127894658	H3K4me1 hESC enhancer GRCh37_chr21:39201385-39202107 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (37829083..37829805)
Select item 127894657 LOC127894657 ID: 127894657	H3K4me1 hESC enhancer GRCh37_chr21:39200662-39201384 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (37828360..37829082)
Select item 127894656 LOC127894656 ID: 127894656	H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:39127657-39128504 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (37755354..37756201)
Select item 126653363 LOC126653363 ID: 126653363	P300/CBP strongly-dependent group 1 enhancer GRCh37_chr21:39345582-39346781 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (37973279..37974478)
Select item 124905070 LOC124905070 ID: 124905070	small nucleolar RNA U13 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (38187457..38187562, complement)
Select item 124905020 LOC124905020 ID: 124905020	uncharacterized LOC124905020 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (38156940..38171700)
Select item 112694745 LOC112694745 ID: 112694745	Sharpr-MPRA regulatory region 8394 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (38171775..38172069)
Select item 110121448 LOC110121448 ID: 110121448	VISTA enhancer hs1811 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (37855304..37856921)
Select item 101928368 LOC101928368 ID: 101928368	uncharacterized LOC101928368 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (37751537..37760512)
Select item 84677 DSCR8 ID: 84677	Down syndrome critical region 8 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (38121451..38156511)	C21orf65, CT25.1a, CT25.1b, MMA-1, MMA-1a, MMA-1b, MMA1, MTAG2	613396
Select item 10281 DSCR4 ID: 10281	Down syndrome critical region 4 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (38054011..38121360, complement)	DCRB, DSCRB	604829
Select item 3763 KCNJ6 ID: 3763	potassium inwardly rectifying channel subfamily J member 6 [Homo sapiens (human)]	Chromosome 21, NC_000021.9 (37607373..37916457, complement)	BIR1, GIRK-2, GIRK2, KATP-2, KATP2, KCNJ7, KIR3.2, KPLBS, hiGIRK2	600877

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