Tag | Content |
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EnhancerAtlas ID | HS061-05299 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr12:26625960-26626930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DMRT3 | MA0610.1 | chr12:26626890-26626901 | TTTGATACATT | - | 6.02 | EWSR1-FLI1 | MA0149.1 | chr12:26626525-26626543 | TCTTCCTTGCCTTCTTCC | - | 6.44 | RARA | MA0729.1 | chr12:26626502-26626520 | CCTTGCCTTTTTGACCTT | - | 6.34 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 26626326 | 26626794 | chr12 | 26626200 | 26626800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I026473 | chr12 | 26625934 | 26626930 |
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Enhancer Sequence | AGTCATGCAC CACCACACCC AACTAATTTT TGTATTTTTA GTACAGATGA GGTTTCACCA 60 TGTTAGCCAG GCTGCTCTTG AACTCCTGAC TTCAAGTGAT CCACCCACCT CAGCCTCCCA 120 AAGTCTTGGG ATTACAGGCG TGAGCCATTG CACCTGGCCT GTATCCTCTA CTTTTATGCT 180 TAGTCTGCTT CAAACTGAAG TTACCTAACA TAAGTCTTTT CTTTACCTTG ATATTTTCAC 240 TGTTACCCCT AAGACACTGG TCATCTGAGA CTGCTTTATT AAATTTCTTA ATGGATGTCA 300 GGTGGTTCAT TCATTGTCTG CTGGCCAATC TGTCACTCTG CTGGCTCCAG GGCAAGCTTA 360 GCTCATCTGG TTGTTCATTC CCCACTCAAC AGCTACACAG TCAGGTTTTA CTCATGCAGC 420 TGCTCACTCG TGCAAGAAGA CAACCTCCCC CATACAAAGC AAGACTATCT TGCAGTCAAG 480 AAAACAGAAG TGGTTCTACT TCCCTACTTT CTTCTTCTGA AACTTATTAC TGCTCATTTT 540 GACCTTGCCT TTTTGACCTT GCTTGTCTTC CTTGCCTTCT TCCCTCCACA GTGCTACAGC 600 CTCTAAAGTA ACTCCTTGAC CCTGTACACA TATGGGTCAG CATGTTTCTG TGTTCATTCT 660 AGTAGCCAAT ATGATTTTAA TTCTCAGCCT GGGATTTTTT CCTTTCTACT CACATTCAAT 720 CTCTAGCCAT TCCTTTGCTA GCTTGACTCA CTTTGTGTCA CATGGCTTCT CTTTCTCTCT 780 AAAACGACAC CTTTTCCACA TCCTAAATCT CCACTTTCTG CTTCCTTCCA CTTGTCCATC 840 ATCCTGGCTT TCAGTTGCTC AGCAGCTAAA ATGCTCATCT GTCTAGCTAT AAGTCATCTG 900 CCCTTACCTC TTTCTGTTCT ACATAGGTAT TTTGATACAT TATGAGAGAC CTTAAAATAT 960 TTTCAATGAG 970
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