Tag | Content |
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EnhancerAtlas ID | HS048-03516 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:225858440-225859910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:225859877-225859898 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | TCF7L2 | MA0523.1 | chr1:225859253-225859267 | GCCCTTTGATCTTT | - | 6.71 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I225670 | chr1 | 225858394 | 225859840 |
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Enhancer Sequence | CAAAGGACAT AAACAATTGA GTCAGTGGAC TGGGAGAGGC AGACTTACCC TCAGTCTGGG 60 TGGGCACCAG CTAATCAGCT GCCAGCATAA AAGCAAGCAT GGAAAGAGCA GACTTCCTGA 120 GTCTTCTGGA CTCCATCTTT CTTCCATGCT GGATGCTTCC TGCCCTTTAA CATCAGACTC 180 CAAGTTCTTC AGCTTTTAGA CTCTTGGACT TACACCAGTG ATTTGCCAGG GGCTATTGGG 240 CCTTTGGCCA AAGACTGAAA GCTGTGCTAT CAGCTTCCCT ACTTTTGAGG TTTTGGGATT 300 TGGACTGGCT TCCTGGCTCC TCAGCTTGCA GACGGCCTAT TGTGGGACTT CACCTTGTGA 360 TCCTGTGAGT CAATTCTCCT AATAAACTCC CCATTCATAC GTTCATCTAT CCTATTAGTT 420 CTGTCCCTTT AGAGAACCCT GACTAATACA AGGCTCTCAT TATCTCCTGT CTAAAATGTA 480 AAATTCTAAT TCATCTCCAG CATAAACCAA GGTCTGATTG TGTCCTAGCC CTACTTATAA 540 GCCTTCCCTG GAGCCCTATT TTCTCAGAAT AAAGTCCACA CTTCTTAGAA TGACATTCAA 600 GGCTTTTACC AAATTAGCCA CAAAAGACTA AAAGACCAAA AGACCAATTT CCTTTAAGTG 660 GGGTAATCTG GGCAGGGTAA TTTTTCTTCC TCACCTTTTC TGCTTGACCC CACATCCTCC 720 ACACATGCAC ATTGGACTGT TGACTCTTCC CTAATTTTCT CACACATGCT CATGGGGTTG 780 TGGCTTTGCT CATGCTGTTT ATCCTACCTG GTTGCCCTTT GATCTTTTCT ACATGACGGC 840 ATGTTCATTC TTTAAGGCTC AGCTCATAGG TCTGCTCTTC TGTGAAGCCG TCTCAACCTC 900 ATGAAGTAGA ATCAACAACT ATTTGTGCTC TTTGGTAGCT CTTAGTCTGT AATGCTCACA 960 AGCTCCTCAC CACAGACTAC TTACTGTATT AGCTGGTTGA GGGGCTCCTG TCTCTCTTTG 1020 CTGGAGCTTA ACTCCTTAAG AACAACGGTG GTATCTTACT CTTTTTACAT CCTGAGGGCC 1080 TCACATTAAC TCCTGCTTAG TAACATGGTT GACTGAATGT GTGGAAGAAT AACTGAGGAA 1140 ATAAATGAAA AGAAATCTGC CTTGGCCGGG CATGGTGGCT CACGCCTGTA ATCACAACAC 1200 TTTGGGAGGC TGAGGTGGGT GGGTCACCTG AGGTCAGTAG TTCGAGACCA GCCTGGCCAA 1260 CATGGTAAAA CCCCGTCTCT ACTAAAAATA CAAAATTAGC TGGGTGTGGT GGCGCAAGCT 1320 TGTGATCCTA GCTACCTGGT ATGTTGAGGC AGGAGAATCG CTTGAACCCA GGAGGCGGAG 1380 GTTGCAGCGA GCTGAGATTT CGCCACTGCA CTCCAGCTTG GGCGACTCCG TCTCAAAAAA 1440 AAAAAAAAGA AAGAAAGAAA TCTGCCTTTA 1470
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