| Tag | Content |
|---|
EnhancerAtlas ID | HS175-29797 | Organism | Homo sapiens | Tissue/cell | SK-N-MC | Coordinate | chr7:127714750-127716260 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr7:127715299-127715311 | TGCAGTGATTTG | - | 7.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCAGCCCAG CTGTGCTCTC CCTGCCCTCC CGTCCTCCTC ACACACTAAT GCTGCTGCCT 60
CCAGAGAACA GGAGGAAGTT CTCTCATCCC CACAGAGTAG CCCAGGAAGG TGTTGGTCTC 120
AGACCCCACA CCAAGGCCAC ACACAGGCGA GGAGAGGCTG CCAGCTGAGG TGTCCTCGGC 180
CACAGCCTGT TGCAGACCTG AGGTGGGCCT GGGCTGCCAG CCCAGAATGT CATCAGTGAT 240
CCCAGGCCTG CTCAGGTGGT CCTGAAGCAG AAATCTGTCT AGGTGACTGT GGAGCCATGG 300
GACAAAATGC CCGGGGCGCC CCTCCCTCCC CAGCCCTGAC CCTTCTCTGT CAGTGCCCTC 360
AGGACTGGGC GGCCCAAGCC CACATCTGAA TTTCCTTCAC ATTGCCCCGT GGGGAAACAA 420
CCCTAGGAGA GGCCTCTAGC TGTTAGGACA AGAGATTTAT AGCCCATCAG TCTCTGTGGG 480
CACCGCATTG AAGAGACAAG GGGGATGGGG TGGAAAGTGG CTTTTGGAAA CCAATTGACA 540
ATTGAGGAAT GCAGTGATTT GGAGGTGGGA GCCGGGCTCA CCCAGCCTGT TGCTTTTGAC 600
TTATAGCCCG GCCCTGATAA TGGGGATAAA TCAGCTGGCC ACCAATTTGT CAGGGCTTCT 660
CTGAGCTTGA GGAGGATTCG TGGGACAGCC GTGCTGAGCT ATAAATTTGT TCCAGGAATA 720
AATGCTTCCT TCCCCATGGG GCAGCCATCT GGCTCAAAAC TCACTTCCCA GAGCTAAGGC 780
CCGGACACCT GCCAAAAAGA GTCGGGGGCT TTGAGGCCCC AGAAGCACCA GATTCTTCAC 840
CAGCCCCAAG CAGCTGCCTC CTCATTCAGG GCATCTCTTG TCCCCTTGGG ACTGTCCTCC 900
TGGGTCTCTC TCTATCTATT CTTCCCTTCC CCTGGGGATT GGGGCAGGCA ACCAGCCCCT 960
TGGTGGTAGA GGAGAGTGGA GGTGGAAAGA CTCCAGGGAA AGGTGGACCA CAAAGCTAGC 1020
ACAGATGAAA GGGACGGTCA GTGCCCTGCA GGAGGCAGCC ACCATCAGAC CTCAGAGGAG 1080
ATTCCCACCT CCTGCTCACA TCAAGCCTCC TCCTCCCAGA ATGAGGGGGA AGCAGGCAGC 1140
CTCAGCTCCT ATAGGAAAGG AGTCACACGG CTTCTTCCTG GATTTCCTGC TTGTGACAGC 1200
TGAACTTAAG ACTGCCACCC CCATGTCCTC TGCCTGCTGC AGGGAGAGGG GGGGAGGGGC 1260
AGCGCTGGGG CCTCCTGTTT AAAGGTTGGC ACTTTCACAG AAGAGTTAGC AGCTGGGGGT 1320
AGAGCGGCAA GCCCCAGAGT CTAACGCCCA GAGGCCAAAA GCATCTTCGT CCTTGCCCTG 1380
CTTCCTGGCT TTTCAGCAGT GAACCTGGAA GCCACCTTTT CAGAGCTGGG CGATCCTCTA 1440
CCCTCTAAGA GTAGAGACTC TAGAGGAACC CAGGGGAGCA CAGGGAGGGG ACTCTGGCCT 1500
GAGATGGAAG 1510
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