Tag | Content |
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EnhancerAtlas ID | HS048-01769 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:87398960-87400410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF7L2 | MA0523.1 | chr1:87400012-87400026 | TTTCTTTGATCTTC | - | 6.64 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_60878 | chr1:87377725-87405070 | DHL6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 87399200 | 87400200 | chr1 | 87399177 | 87400265 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I086933 | chr1 | 87398853 | 87400779 |
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Enhancer Sequence | TGATATTCTC ATTATCCATA GTTACACCTT TTGTAATTGT CCAACAGTTC TTAAATATTC 60 TGTTACTTTT TAAAAAAATT CTTTTTGCCT TTCAGTTTGG GAAGTTTCTA TCAACGTATC 120 TTCAAGTTCA CTGATTGTTT TCTCTGCTGT GTCTAGTCTG CTGTTGAATC CGTCAAAGCA 180 TTCTTCATTT CTGTTACTGA TTTTTGTTAT TTCCATTTCA GTTTGTCTTA GAGTTTCCAT 240 GTCTCTGCCT ACAGTGGGCA TCAGTTTTTG AATGTCGTGT AGTTTTTTCC ATTAAAGCCC 300 TTAGCACATT AATTATAGTT ACTAAATTCT CACAGTGATG ATTCCAAAAT CTCTGCCATA 360 TATGAGTCTG GTTTTGATGC CCGCGTTGTC TTTTCAGACT CTGTTTTTTG CCTTTAGCAT 420 GCCTTGTAAT TTTTTTTTTT TTTTTTGATA AGCTGGATGT GACATAAGGG GTAAAAAGAA 480 CTGAGATAAA CAGGCCTTTA GTGTGGCCTA GAGGCCTATC TGGCTAGGAG TTAGGCTGTG 540 TTTACTGTTT GATGTAGCTT TGGTGTCAGA GATTAAAATT TCCTCTCGTG TAACTGCTTT 600 TGTCTCCTTT GTTGTCTTTG GGTTTCCCTA ATAACTCCTT CATAAGTAGG TTCCGAGGCT 660 TGTAGTTATT TAAGCTGTAA GTCCCTGTTA TTACACAGGA GCCCTATTGA TGTGGTGTGT 720 GTGTGTGTAA AAGTGTTCTA TAATCTTATG ATTAGCTCTT AGTGAGCCTG TGTCTTTGGA 780 CTGTGACCTT CATGAGTGCT TTTTAGCTCC TGCAACCTTT ACCTCCCAAT ACTTAAGTGA 840 GAAAGTAGGA AGGCTGGGAG GCGGCTGGAG TTTTGTATTT CTCTTCCCAC AAGTTGGTTA 900 GTTGGTGGAT AACAAACTGG AATGTGAAAC CTCGGATGAG GGGAGGCTAC TGTAGTTTCT 960 TTTGAGGACA GGTCTTTGTT ATTGAGAACA GAGATCGCTG GGCAATTTCA GAATGGTTAT 1020 TTTTTCTCTC CTATTGGAAG CTAGAGGGAA TTTTTCTTTG ATCTTCACTT GTGAATCTCT 1080 GATGGGGCAC CTGGAGGTAA AACTCAGGAA AGTTTCCTCT GTCTCTCCCC CAGCCAGACT 1140 GCCCATCCCC TGAGCTTTTA ATTCTCAAGC TAGTCCACGT TGAACCTCCA GCAATTTACA 1200 TTACAGTGTT CCTATGGATA CTGGCTCCAG CTGTTTGTTT CTCTTGCTGG GGTTTGTGAT 1260 ACCCGTAGCT GTGGTTTTCT GTAGTCACAT CTCTCTCCAG TTTTGGGAGC AGCAGTTTGC 1320 CCTGAACCTC AATTCTCTAT TGGGTCTAAG AAGAGTTAAC TGATTTTCGG CCGGGCACGG 1380 TGGCTCACGC CAGTAATCCC AGCACTTTGG GAGGCCGAGG TGGGCGGATC ACCAGGTCAG 1440 GAGATCCAGA 1450
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