Tag | Content |
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EnhancerAtlas ID | HS191-19608 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr2:10915200-10916320 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr2:10915265-10915286 | GTCTCCAGCTCTCCCTCCTCC | - | 6.49 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 10916003 | 10916120 | chr2 | 10915379 | 10915482 | chr2 | 10915629 | 10915870 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I010772 | chr2 | 10912874 | 10916394 |
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Enhancer Sequence | AGTATGTGAT TGAGCAGCTC CTCCCGCCCC TACCCGGAGG CCTGGGGATA GAAGAGTCCT 60 CCCAGGTCTC CAGCTCTCCC TCCTCCCTCT CATTGTCCCC AGGCTCCTGG GCTCACACCA 120 TGGGGACCGT CTGTTCTCAT GGGACGCCTG AGCAGGGTCT GGGGGGAGGG GCGGTGAGCA 180 CAAAGGAGCC CAGGCGGTGG AGCTGGGGGC GGGAGCCGGG GGCCCACCCA AGCTGGCGCT 240 TTCCACATGT GTTCTCACTG GTCCTGAGCA CCGCCCTGCC AGGAAGGGGT TGCTAGCTCC 300 ACAGTATGGA GAAACTGAGG CTCTGAGAGG CAAGCTGGCC AGAGGACCCT GCCAGGCCTT 360 CCTTGGACTG AGCAAGGCAC GTGGGCTCCA GGCGGGAGCA TCTGTGTGCA GGGTGGGCAG 420 TGCTGGGCCT TGGAGATTGC AGCCGTGAGG TTTCCAGGGC GCCACTAGCC CCTGTATTTA 480 CCTCCCGTGT CCTTAGTGCG GAGAGGGTGC TTATCTGGAG ACTTCCGACC ACAGCCACTC 540 AGAAACCCTT CACGGAGGAG GACAGCGTAG CTCACCAGGG AGCAAAACTA GATGCTCACG 600 TTTGAATTGT GAGCAGGAGA GCTTTGGGAA GGTCCCTCCA CCGCTCCGGG AAGTGGGCAC 660 CTTCCATACT CAGGTTCTCC TGCTGCGATG CTGGGCTAGG CTGGGCAACT TGGAAGGAGC 720 CTGTCTGGGT GGAATGTTTT TGGGACCCTT CTTCCTCATG CCCACCAGGG AGGGTTCCGT 780 GAGCACCTTC CAGTCCAGCC TCTAGTGACA GGGCAGGAGG AATGAGTAGA AAGTTCTTGA 840 GGCCTTTGGG GGAAAGTCAC TGTGTGAACA CAGCACTGTG AGGACTCCCA TGGGGAGGAG 900 CGCCGTGGCC GCGGGCAGGC TGGGAGTGCT CCCAGTGTCC GTGCTGCCAA GTGTGTGCTC 960 CGGGCTCCTG GGGACCTGGC CTGTCTGTCA GCGACCTTTT TGCAGGGACT GGGGATGAGC 1020 AGCCACCCCG TCACAAGCGA GCCCAGCCAC GGAGCCCCCG TAGTGGGGTT CTCGGAGCCC 1080 CTCTGGTCTG GTCTGTTTCC CTTTAGGGAG GAAACAACAG 1120
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