| Tag | Content |
|---|
EnhancerAtlas ID | HS095-23101 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr4:142052000-142053470 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr4:142053385-142053396 | CTTCCCAGAAG | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH04I141130 | chr4 | 142051556 | 142052153 |
| Enhancer Sequence | TTAAGACTCA AGGTGAGAGC ACAATCTTTT CCCTTAGAAA ACTGTCGAGC TCAAGAAAAT 60
ATATCGAATA TTCTGAAAGT GCTGTATTGT AACTTTTCTA AGTAATTGCC TCTCCTCCTC 120
TTCATTAATT AACACACTAC ATTTTTCTGG CCTGTGTTTT AGAAGTCTGG AACATTTCCC 180
CTCCCCACCT GTTTGTGTTA AGGTTGACAA ATTTCCCTGA CTAAAACAGC TGGTGTTGAT 240
TACTGGAGGC AAACCAATTG AATATTTCAC TAATAGGTGA CATGAGCTCT CGGAATGGAA 300
ACTTGTCCCC AAAGAGAACA CCCCTACAAA TGTAGCCAGA GCTTGGTGTT CCATTTCAGC 360
AGCGTAACTA TTTATTCAAA TTTGGTTTTT AAAGAAAATA ATGCTTTTGA TTAGGAGACT 420
CCACTCAGAA AATGCATCTG TCATTTTCTC CCCTCCTTCC GGGCACTGGA TGCCACAGTC 480
TCGGCCCAGA AACCCCTTTG GGGAAGGAGG GCCCACTTCT CAGGCACACA AATACAAGCA 540
GCAAGCTCTG ACATAAGGAG GCTAGCTTGC TAAAACTAGT GGCTTATGGA CTTATGTTAA 600
CAAGCCTGGG GATGGCTTTT TTGGGGGGAG GGTGTTCCTA CCACCAGGGA AACATTGCTT 660
ATGTCAGGCA TATGCGGTAT TGAGTTTTGG GACAGTAATG CATTTCTAGT CCTGGTACCT 720
GCGATCATTA ACAAAAGCTT ATTCTCTCTA GTCTGAAATC CCTTCATTCT AGCCAGAAAG 780
AAAACCTTCA GCATATTTAA CCTCCCAATC AGGCAAAGGA TAATGCAATA ATTAGAAAAG 840
TAGTTATAAC TTTAGGGCCA TCACACTCTT CTTGGCTTGT TGAGGATTGT TATTATTTAC 900
CATCGTGGCC ACCTGTCAGT TTCTCTGGAT GACAGCCTGG CAGAGCATAG TACTTTTAAT 960
ATGATTAATG AAGTGCGTAA ACCCAAAAGG GGAAACTCTC CCAAGTGCAA GTTCGCGGTG 1020
GTGAGCTGCC AGCAGGTAAC CCTACCCCTC TCCTGATATA GCGCCTGCAT CAGGGTATAC 1080
CTGATGCACA GACCCAAGGG CAGTGCTGTG GTATCAGATC TACTGGTTCC AAACAGGTGC 1140
TGGGCCGGTC ACTAACCAAG AACAGTATCT GAGCCCTACC CTCCAAACCC CACCTTCCAG 1200
GTCCCCCTCG GAAAAGTTAG CCCGCCACGT TGAACCCCTG TCCAAGCGGC GCTATGCCAA 1260
GCTCTCCGGC AGCCTCTCCC CTACCCAATA CAGTTAATCT TCTCCTCTTT GTAAACCCCC 1320
CAAGTGACGC GGAGCAAAAC TTAATCGGTC CAGGGAACCC AGACACGTCT TCCGCGCCGC 1380
ACGGACTTCC CAGAAGGAGC CTGGAGGCAG GCGCTGGATC CCTCTAGGCA CCTCCGTCCC 1440
CGCCGGCTCC CCTCCCCCGC GCCCGCTGGG 1470
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