| Tag | Content |
|---|
EnhancerAtlas ID | HS048-26980 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr3:186981680-186982870 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr3:186982035-186982047 | GTGTAAACAGAA | + | 6.22 |
| | | 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 |
| GH03I187261 | chr3 | 186979738 | 186984050 |
| Enhancer Sequence | CGTATCTATT CGATTATCTT ATACCTAATC CAATTCTTTT AAGTTGTATT TGTGTTTGCA 60
ACCTCTGGAC CAAATTTTAG CCAAGATGCA TGAAAAAAAT CTCTTACCAA GAATGATTCC 120
TGCTGCCTTT CAAAGTCATT AGAGAAAAGT TCTCAAAGGC GGCTATCTCT AGTAGCTTCT 180
AATGAATTCA TTGTTTTGTT CGTTAGCTTA GCATGTCAGA AATATCTTGA CATTTGACAC 240
TCCTGTTTTG AAACTAATGG TTTATTTATT TAAAATAAGT GGGAGTTTCA AAGAAAAACA 300
ATTTGCCCTG GCAACAAAAC GCAAGTACAA TTAATCACTA ACTTTGGGAA TTGAAGTGTA 360
AACAGAAGAT GAGATCATGG CTTTGCTATT TATTCCTCTT CTCTGCAGAT ACCAGCCGAA 420
CTCACACCAG TCTTGTTACT ATAGAATGTG CCTATCTGCA CACAGCTGAA ATGTCACTTC 480
CTTGAACCTC CCAGCTGCTG TTTTATTTTA TCTGACTCAG TTTTCCAGAT AGCCAAAGCT 540
TTACCTAACT ATAACTAAAA ATTTTCTTTT TGGTGTAACA CTTAAAAAAA AAAAAGTACT 600
TTAAAGAAGT ACCCACTTTC TCAAGTGAAA CATGCTAACC CTTTCTTGGT GATCCAGGGA 660
CATTGTTATG AATGTCAACC ATTGTGATAC TATATTAAAG TGATAATCTT GGGGATATTG 720
AGTTGTGTAA TGTCGCTTGA CCTGGCGTTA AACATTGCCG GACTATAAAG CCTTGAACTT 780
CTGAAGTCTT CTTTATGTCA TGTTTTATTT CCTGTCTTTT TATCAGCCTA TTCACTGTAC 840
TTTTCTGTCT GCTTATTTTT AATATGTTGT GAATTAGAAA CCAGTTAACT GCTTTTGCTA 900
GAACTTAATA AAAAAAAGCT AAATAGATTT AGAATGAGGG CCTGGGAAAG GGATTCTTCT 960
GTGAGTAACT GCATGAACTA GAGTACACCA TCTTGGTGAC CTCTGCTTTG GAGTAATACG 1020
ATATACAGGA ACCTGGCAGT TGGAGGTCCT GGGTCCTGTT CCTGACACTG CCGTATTCTG 1080
CATTTTGGGC CATCTCCTTT CTAGCTCTCA GTTATCCACT TGTAAAAACA GGGGTTTGGA 1140
CTAGCTGAGC TCTAGATTCC TTTCCAATTC CAGACATAGC AGTCATCATA 1190
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