Tag | Content |
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EnhancerAtlas ID | HS108-27679 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr3:32115320-32116810 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Tcf12 | MA0521.1 | chr3:32116250-32116261 | AACAGCTGCTG | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCGCCACTCT TGACTCCCTC TTGGAGTGGA TAGATGATCT TTTCTGACAG GGCACCCTCC 60 AATACTTCCG CCCTGATGAA GTTCTATCCT TTACTTTTAT ACTCACTCTT ATTCTCATTC 120 CCATTCTTAT GCCACTCTCT ACCTCTCCCT AGTTACCTCC AGCATACTAG CAATCTCATC 180 CACTTTGTCC TCACTGCCGC CAATCCTTCT CTAGCAAAGA ATTGTTGGCT ATGCATTTCC 240 CTTTCTTCCT GCTCTTACAC AGCCATCCCC GCTCTACAGG CCGACTGGGC TACCTCTCCC 300 ACCTCCCTGC ACCTCAGAAC CTCCTTTAAT AGCCCTCACT TTACCCGCCT GAGGAACTTC 360 TTTACTTTCT AGACAGATTT GGTGAGAACT CCCCAGACAT TTCACATCAA TAAGCTGTCA 420 CACTTCTCCG CATCTACTTA CGGCACCTTT CTCCTTATGT CAATTCCACG CCCCCATATT 480 TGGACTGCTA ACCACGCAAA CAACTATCCC TGTTGCCACT CCTTTATGCA TCTCTCGACA 540 ACAGCCTACT GGAATCCCTT TAGGCAACCT TCCACTGTCC AAATGTTCCT TTACTCTTTA 600 TCTCCAGAAC CCAGCCACAC ACATTACCAA ACAGATGGGA GCATTCCAAC TTCACGTTAC 660 TGATAAGCCC TCTATCATTA CTGACAAACT GAAAAACATT GGCAGTCACT ATTGTTTAGG 720 AAGACACCTA CCCTGCATCT CACTGCATCC TTCGCTACCC TCCCCCTGCT CATCTGAATC 780 TCCTCCTAGC CCCTCCTCTT GCTTGCTTAT ACCCAGCCCC ATGAATAGCA GTGAAAGGTT 840 ACTTGTAGAC ACTATGCACT TTCTCATATA CCATGAAAAC CGAACCCCTC CCTCTATGCA 900 GTTGCACCAT CAATCCCCAT TACAATCTGT AACAGCTGCT GCCCTTGCTG GATCTCTAGG 960 ATTTGGGGTG CAGGATTCCT CTTTCAGTAC ACCCTCTAAC CTTTTCACTT TACATTTCCA 1020 GTTCTGCCTG ACACAAGGTC TCTTCTTTTT ATGCGGCTCT TCCACCTACA TGTGCCTACC 1080 TGCCAACTGG ACAAGCACAT GTACTCTAGT CTTCCTTACC CCCAAAATCC AGTTTGCAGA 1140 TGGGAATGAA CAACTGCGGG TCCCCCTCAT GACGCCAACA CGACCAAAAA GAGTCATCCG 1200 ACTAATCCCT TTACTTGTGG GTCTACGACT TTCTGCTTCC ACTATTGTAC TTGGAACTTG 1260 AATAGCAGGC ATTTCAACCT CTGTCACAAC ATTCTGCAGC CTCTCTAATG ACTTCTCCAC 1320 TAGCATTACA GATGTATCAC AAACTTTATC TGTTCCTCAA GCCCAGGTTG ACCCTTTAGC 1380 TGCAGTTGTC CTCCAGAACC GCCAAAGCCT TGATTTACTC ACTGCTGAAA AAGGAGGACT 1440 CTGTATATTT TTAAATGAAG AGTGTTGTTT TTACCTAAAT CAATCTGGTC 1490
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