Tag | Content |
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EnhancerAtlas ID | HS105-45050 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr2:113603090-113604390 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr2:113603249-113603263 | CCCGCCTCGGCCTC | + | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGCCTCCCG GGTTCACGCC ATTCTCTTGC CTCAGCCTCC CGAGTAGCTG GGACTACAGG 60 TGCCCGCCAC CACGCCTGGC TAATATTTTG TAGTTTTAGT AGAGATGGGG TTTCACTGCG 120 TTAGCCAGGA TGGTCTTGAT CTCCTCACCT TGTGATCCGC CCGCCTCGGC CTCCCAAAGT 180 GCTGGGATTA CAGGCATGAG CCACCGCGCC CAGCCAGACC TCTTGAGTCT TAAACTCCTC 240 TGTAGTTCCA GCCACCCTTT AGCACATGAC TCTGTTAATT TTGTTCTCAC TGTCTGAAAT 300 CATCTCCTGT CCACTCTTGA CTGACAGGTC TCTGCACTAG CCCACTGCTT AATCAGAGTA 360 GGTCCCTGTC AACTTATTCA TATTGTGTCC CCATGCCAGT GTGGATGATT AAAATTGTTG 420 AGTGGAGGCT GATCAGATGA GCCATCTCCT TCCAAGTCCT CACTTGCTGG CTCCTGTCTT 480 AGTTTTAGTC CCCATTCTTC AAAGAACGTG AGCCCTGGAA AGTATTTTAG TCATTTAGTT 540 CAGTGCCTTT GGATGGGAGG ATCACATCCC TGGGTCCCGT CCTGCAGACT GTTTTGCTCT 600 AGCTGACTAG GCAGGATTCC CTGCCTTCTC TCACTTCTGC ATGGGACTTC CTTCTGAAAT 660 TGCTGCTCAG TCAAGAGAAT GACCTTCCCC AACATAATCC TACTCCACAG GGACTTAAAG 720 GTGTGTCAGA GATCTCTTGC TCATCTTTCT GGCCAGGTGC CAACGTCAGT TTATAGCCAA 780 GGGACAAGAC TAGTTAGCAG ATCAGGCAGG TCTTAGACCC CAGCGTAAGT GCCAGACTTC 840 TAGCTGCAGT TGTTCCTGCC CACACTGGGC GTTCAGGTGG AGAGAGGGCA TGGCACTACA 900 CTGAGCTCTC GGCGAAACCC AGGACTCTGA AATCTCGGTG TCAGCCCCAG GCCACTCTCT 960 TCAGCAGAAC TTCAGTCAGT CCTGTCACTA GGAGATGGGA CCCTGCCTGA TTGCATTCTT 1020 ACAAATGGCT ACATTGACAA GGGGACTAGA CTTGACTGAG TGGAGATTGG GGGAAAAGGA 1080 AATAAGCCCT CAGTGCTTTC TCTGAGCACA TCACCCTTGC TGGCTTAGCA TCTATTGTTT 1140 GTCAGAAGAC TTAGCTATTA TCTTGGCAAA TATTCTCTGC TTGACCAAAT TTTAGTCAGG 1200 CTCCTGAACC TTCTCCCAGG CACATTTGTA CACTTTCTTG TAAACTCCTT TTTTAGCAAG 1260 AACCTTCTAT GTTCAATATC TGATCACCCT TGAAATCTCA 1300
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