| Tag | Content |
|---|
EnhancerAtlas ID | HS138-30061 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr4:74641220-74642580 | 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 | CAGAAACTTA ATAGATACTT AGTTTCATTA GTTATCAAAA AAAATCAAAC TTAAACCACT 60
ATGAGATAGC ATTGCATATC CATCAGATGG TCAACAACTG GTAAATCTGG TAACACTGAA 120
TTTTGGTGAG GATATGGGAA AATGGAAATT CAGACATGGC TGGGGTAAAT ATAAATGCAC 180
ATAACTTTGG AAATTGGCAA TATCTAGTGA AAGCTGAAGA TATGCAGAAC TTACCCCAGC 240
ATTATCCCTT CTGCGTCTGC ACTAGAGAAA TCTTCAACCA TGTACATAAG AAATTGCTAT 300
AAGGATGCTT GTGAAGCAGT GTTGGTAATA GCAAAAACTA TTGAACCTCA GGAGTAAAAT 360
TCATAAACAG TGCAATGATA GAGTTAAAAT GAAACTACTC AATCTAACTG GTTAAACAAG 420
GGTAAACCTT TAAACATACT TCTGAGTAAA AAAGAATACA AAATGCTACA TCCAGTACAA 480
TGTCATTCAC GTAGATGTTA AGCACTAAAT ACTATATAGA GAAACATGAA TCTATGGTAA 540
AAGTTCAGAA CACTAAAGAG AATGATACTA TCATCACAGG ATTTGAATAG TGAAGAGAGA 600
AAACTGGCGA ATGGGACTTT AGAGTCTATG TATTTTTTAA TTAAAAAAGA TTGGAATCAA 660
TTATAATCAA ATATTAATAG AGCTAATCTC AGAGGTGGGT AGATAGGTAA TGGTTATATG 720
CACATATATT TTACTTTTTT GAATAAAATG CTTTATAATT GAGGTCTAAA AGGGTAATAT 780
GTGTGGAATT TTTTTTTTGG CAGGGGAAAA TAAGGGGATT TAAATCATTT CTTCATCAAA 840
AATCCCTTTG AACTTTTATT TGCCAAACTT CCTTCTTCCT TGTTATGAAG ATTAGTAACT 900
CCAAACCATA TTCACTTCTG CGGTTTCATT CTGAAAAAAG AAAATTTGGC TGGTTTAGAT 960
AAAGCATTCC ATTAACCTAC ATTCTGAACT AGATGTTCTA AAAGGAAGTT ATTATTTTCT 1020
CTGGCAGAGA TGAAGGGAAA AGCCAAAACA TTTTGATGTT GACACAGCTT TTGGAGAAGT 1080
GCCAAAAAGG TCACTGAGTC TGTGATCCTT CATGGTGTCC GCAATGTGGG CCTTGCAATG 1140
ATCCCAGTCC TGCTTACCAC AGGGTGCAGG TGTCTTTGGA GCTGAGTAGA AACATTCTGA 1200
AAACATGCAT GTTGCTGTCC CTGGATAAAT GCTTAATACT TAATGCACTG CTTTTCCTTG 1260
GTCTCAAAAT TGTTCTTAAA CTTACTTTGT GTGGCTATCT CAATGTTTAT AAGCCAAAGA 1320
AAGCCAGCTA CCTATTGCTT ACTGATGGTA CACTGCATGT 1360
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