Tag | Content |
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EnhancerAtlas ID | HS060-31873 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr7:74012890-74014440 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF3 | MA0522.2 | chr7:74013722-74013732 | AACACCTGCT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGAGATCACA CTACTGTACT TCAGCCTGGG GAACACAGCC AGGCTCTGTC TCAAAAAAAA 60 ACAAAACAAA ACATGGCAGA GACACAGAAG GCCACATGAA AGCCTCAGGA GGATTTGGGA 120 CAGATGCCCA GAGGGTGGAT ACTGTCACCC ACATCCACCA CTCCCTCCAA TGTGGCCATC 180 TCTCATGGTG ATTCAAGGAT GGCCACAGCC CATGGACCAG TCTGAGACAG AGGGTGGGGC 240 AGCCTCTGAC TTCTTTTTCA TGTGGAATCT CCCACAAAAA TCCCTCTGAC TCATAGCCTG 300 GGCTCCTCCT GCCTCCAGGG TCTTCTCTTT CGCAGGGTCT CTATGCCTCA CCACAGACCC 360 CCAGTTTCTG ACTTCTCCAC CAGTTGAAGA GACATTTGCC CCATGGACCC AGCCTGCCCT 420 TACTCTGTGT CATTAAGACC CTTCCGGTGG GCTGAGTGCA GTGGCTCACG CCTGTAATCC 480 CAGCACTTTG GGAGGCTGAA GCAGGAGAAT TCTTTGAGCC CAAGAGTTCA AGACCAGACT 540 GGGCAACATA CAGAGACCCC GTCTCTACAA AAAATTAGCC AGGCAGGGTG GTGTGCACCT 600 GTAGGGAGGC TGAGGCAGGA GGATCACTTG AGCTTGGGAG GTGGAGGTTG CAGTGAGCCA 660 AGACCACACC ACTGCACTCC AGCATGGGTG ACAGAGTGAG ACCTTGTCTC AAAAAGACAA 720 TAAAAGCCCT TCTTTATTGG GCTGGGCGAG GTTTCCATGC AGTAATCCAT CCAATCAGGA 780 CGTGCTGCTC AAAGTCTTAC ATCTTCACCT CAAGTTAATC CAGCAACCAC AGAACACCTG 840 CTGACCCCTC CTCCGTGCTG AACTAGGTGC TGGGTTCTTT TATGCATGCG GTGTTTTTTG 900 AGTCTCACAT CACACTGGTT TCCCCATTTG ACTCAGAGAG GTTCATCAGT TTTCCCAGAT 960 TCACACAGTG ATAATAGTAA GTGGCCACAG TGAAATTTGA ACTTAGGACT TCTGATTCTA 1020 AACCAGAGTT TCTTTCACTG GGGCACTGCC TGTCTACTTG GACCTGTGAA CTCTCCACTC 1080 AGGACCACCA TACATTAGTG ATAACCATAG CAATACAATT TTTTTGTATT TTGGTAGAGA 1140 CAGGGTTTCA ACCTTCACCA TGTTGCCCAG GCTGGTCTCG AACTCCTGAC CTCAGTCAAT 1200 CCACCCACCT TGGTCTCCCA AAGTGCTGGG ATTACCAGTG TGAGCCACTG CGCCTGGCCC 1260 CAGGTCCTCT TTATACCCTC CCTGGACAAC CTAGCCTGCA GTTCCAGCCT CCCCAGAACT 1320 CCCAGAGCCT CTCCTGGGGT CCCACATCCC CTCACAGCCT TAAAGAGCCC AGGAAAGAAT 1380 GTGGCCTCCG GAGCCACGCA GACTTGGCCT TGGAGAAAGT CCTTTAACAG CCCTGCCCCT 1440 TCGGGTGCTC GTGAGTGAAA TGTGAATAGG ATCTTGGAGG GTTGCTGGGA GGATCCCAGC 1500 AGACAATGTG CAAAGCATTT AGCACAGTGC CCAGCACCCA GAAAATACTC 1550
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