| Tag | Content |
|---|
EnhancerAtlas ID | HS105-76800 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr8:21946810-21948120 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIC | MA0161.2 | chr8:21947692-21947703 | TCTGCCAAGAA | - | 6.02 | | ZNF263 | MA0528.1 | chr8:21947815-21947836 | CTCCCCACCACCTCCTCCCCA | - | 6.01 | | ZNF263 | MA0528.1 | chr8:21947024-21947045 | CCCACCTCCCCGGCCTGCTCC | - | 6.09 | | ZNF263 | MA0528.1 | chr8:21947806-21947827 | CCCTCCTTCCTCCCCACCACC | - | 6.22 | | ZNF263 | MA0528.1 | chr8:21947812-21947833 | TTCCTCCCCACCACCTCCTCC | - | 6.41 | | ZNF740 | MA0753.2 | chr8:21947662-21947675 | GTGGGGGGGGTGC | - | 6.74 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGAGGCCGGC AGGGCCGGGC CGGGCCGCCG GGAGTCGCGG GCCTAGGCCG GGCTGGGCGG 60
GCGCGGAGCC GGGCGCGGCC CGCAGGAGGG CGGGCGGGCG CGGGCCCCCT CGGGCAGGGA 120
CCCCCGGGCC GCGGCGCCCC TTCCTCTGCC TCCCCGGCCG CGCCCCGCTT CCCCTCGCTC 180
TTCCCAGTCC CGCTCCCAGA CTCCTCCCGA CCGCCCCACC TCCCCGGCCT GCTCCCGCGT 240
CGCTTCCTGT CTGTGCGTCC TGGCCCCGGA GTCTCTCCCA ATTCCCGAAC TCGCCTCCGC 300
CGGGACGCTC CCTGTCACCG CTTGGGGTGT TTCCTGCCCC CCGGGGCCCT AGGCCGCCTC 360
CCCCCAGTCC CGGTGGGCCT GCCTCCTTCC TCCGCTCCAC CCCACCGCCT CGCCTGGGCT 420
TGAAAAAATC GCCGTCCCTT CCCCTCGGTC TGATCTCCCA GACAACTCCA GGACCTTGTT 480
GGGGTGCAGG ACGCCCTTCC CGTCACCCCG GGACGTGGGA AGTGCAGGCC CTGCCGGTCC 540
AAGTCCCCAC GAAGGGTAAA GACCCGGGGC AGGCTGGTGG GCCCCCAGCC GGGGAAATCG 600
CCTTCTATTG GGTGCAGATG TTTCCAGCGT GGCTGTGACC CCTCACAAGC CAAATTGAGT 660
TAGGGACATG CCGCCCGTGG TGGGGCCTGG GTGGCCCTGT GCGGGGAGGA GAGTCCATTG 720
ATGTTTCACG TGCCGTCAGT TTGTGTTTTT GCCATTTTTT GTTGGGGCTG CAGGCTGGCA 780
GGCAGCCTAC TACTAGGGTT CGTTCAGCAA GATGTAGCGC TGTGTAGGAA GGGTGGGGGT 840
ATTCCCGGTA GGGTGGGGGG GGTGCCCGCT GTTGAAAGTA ACTCTGCCAA GAAGCTGTCT 900
GTAAAGTCAG CAATACTTCT GCCTCCTAGT ATAAATCTTC CCCCAATTGA TGAGTTGAGT 960
ATCAGATTTT CTCAGGAGAG AAAGTCTTGG GTTTCACCCT CCTTCCTCCC CACCACCTCC 1020
TCCCCAACCC TCATGGGAGC TCCTGTTGAA AGAAGTTTGC CTTAGGCAAA GTTGGGAAGA 1080
AAGTCAGAAA CTATGACTTC CTCCACCTTC CCAGCCCTGC TGTTGACCCA GGGCCAGGGC 1140
CTTGGGGCAT CCAGGTAGAG AGGGTTCCAA AATGATTTTT CTTCCCCTTC CCCCATCCCC 1200
AGTCAAAACA GCTGTGATCT TCAAAAGTGA TCTGATAAAC CAATTCATAC CTCTGGGGAA 1260
CACTCCATTT ACAGGAGGTG AGACAGGCCA GACAGTTCCT CAGTCCTGAG 1310
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