| Tag | Content |
|---|
EnhancerAtlas ID | HS118-14181 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr4:74641200-74642610 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr4:74642062-74642076 | TCCCTTTGAACTTT | - | 6.78 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH04I073776 | chr4 | 74641927 | 74642201 | | GH04I073777 | chr4 | 74642317 | 74642518 |
| Enhancer Sequence | GAATATGAAT AGGCAATTCA CAGAAACTTA ATAGATACTT AGTTTCATTA GTTATCAAAA 60
AAAATCAAAC TTAAACCACT ATGAGATAGC ATTGCATATC CATCAGATGG TCAACAACTG 120
GTAAATCTGG TAACACTGAA TTTTGGTGAG GATATGGGAA AATGGAAATT CAGACATGGC 180
TGGGGTAAAT ATAAATGCAC ATAACTTTGG AAATTGGCAA TATCTAGTGA AAGCTGAAGA 240
TATGCAGAAC TTACCCCAGC ATTATCCCTT CTGCGTCTGC ACTAGAGAAA TCTTCAACCA 300
TGTACATAAG AAATTGCTAT AAGGATGCTT GTGAAGCAGT GTTGGTAATA GCAAAAACTA 360
TTGAACCTCA GGAGTAAAAT TCATAAACAG TGCAATGATA GAGTTAAAAT GAAACTACTC 420
AATCTAACTG GTTAAACAAG GGTAAACCTT TAAACATACT TCTGAGTAAA AAAGAATACA 480
AAATGCTACA TCCAGTACAA TGTCATTCAC GTAGATGTTA AGCACTAAAT ACTATATAGA 540
GAAACATGAA TCTATGGTAA AAGTTCAGAA CACTAAAGAG AATGATACTA TCATCACAGG 600
ATTTGAATAG TGAAGAGAGA AAACTGGCGA ATGGGACTTT AGAGTCTATG TATTTTTTAA 660
TTAAAAAAGA TTGGAATCAA TTATAATCAA ATATTAATAG AGCTAATCTC AGAGGTGGGT 720
AGATAGGTAA TGGTTATATG CACATATATT TTACTTTTTT GAATAAAATG CTTTATAATT 780
GAGGTCTAAA AGGGTAATAT GTGTGGAATT TTTTTTTTGG CAGGGGAAAA TAAGGGGATT 840
TAAATCATTT CTTCATCAAA AATCCCTTTG AACTTTTATT TGCCAAACTT CCTTCTTCCT 900
TGTTATGAAG ATTAGTAACT CCAAACCATA TTCACTTCTG CGGTTTCATT CTGAAAAAAG 960
AAAATTTGGC TGGTTTAGAT AAAGCATTCC ATTAACCTAC ATTCTGAACT AGATGTTCTA 1020
AAAGGAAGTT ATTATTTTCT CTGGCAGAGA TGAAGGGAAA AGCCAAAACA TTTTGATGTT 1080
GACACAGCTT TTGGAGAAGT GCCAAAAAGG TCACTGAGTC TGTGATCCTT CATGGTGTCC 1140
GCAATGTGGG CCTTGCAATG ATCCCAGTCC TGCTTACCAC AGGGTGCAGG TGTCTTTGGA 1200
GCTGAGTAGA AACATTCTGA AAACATGCAT GTTGCTGTCC CTGGATAAAT GCTTAATACT 1260
TAATGCACTG CTTTTCCTTG GTCTCAAAAT TGTTCTTAAA CTTACTTTGT GTGGCTATCT 1320
CAATGTTTAT AAGCCAAAGA AAGCCAGCTA CCTATTGCTT ACTGATGGTA CACTGCATGT 1380
TAATTTATTA TTTTTGGCTT ACCTAATACA 1410
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