Tag | Content |
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EnhancerAtlas ID | HS101-04086 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:225858860-225859840 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
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 | CTGTCCCTTT AGAGAACCCT GACTAATACA AGGCTCTCAT TATCTCCTGT CTAAAATGTA 60 AAATTCTAAT TCATCTCCAG CATAAACCAA GGTCTGATTG TGTCCTAGCC CTACTTATAA 120 GCCTTCCCTG GAGCCCTATT TTCTCAGAAT AAAGTCCACA CTTCTTAGAA TGACATTCAA 180 GGCTTTTACC AAATTAGCCA CAAAAGACTA AAAGACCAAA AGACCAATTT CCTTTAAGTG 240 GGGTAATCTG GGCAGGGTAA TTTTTCTTCC TCACCTTTTC TGCTTGACCC CACATCCTCC 300 ACACATGCAC ATTGGACTGT TGACTCTTCC CTAATTTTCT CACACATGCT CATGGGGTTG 360 TGGCTTTGCT CATGCTGTTT ATCCTACCTG GTTGCCCTTT GATCTTTTCT ACATGACGGC 420 ATGTTCATTC TTTAAGGCTC AGCTCATAGG TCTGCTCTTC TGTGAAGCCG TCTCAACCTC 480 ATGAAGTAGA ATCAACAACT ATTTGTGCTC TTTGGTAGCT CTTAGTCTGT AATGCTCACA 540 AGCTCCTCAC CACAGACTAC TTACTGTATT AGCTGGTTGA GGGGCTCCTG TCTCTCTTTG 600 CTGGAGCTTA ACTCCTTAAG AACAACGGTG GTATCTTACT CTTTTTACAT CCTGAGGGCC 660 TCACATTAAC TCCTGCTTAG TAACATGGTT GACTGAATGT GTGGAAGAAT AACTGAGGAA 720 ATAAATGAAA AGAAATCTGC CTTGGCCGGG CATGGTGGCT CACGCCTGTA ATCACAACAC 780 TTTGGGAGGC TGAGGTGGGT GGGTCACCTG AGGTCAGTAG TTCGAGACCA GCCTGGCCAA 840 CATGGTAAAA CCCCGTCTCT ACTAAAAATA CAAAATTAGC TGGGTGTGGT GGCGCAAGCT 900 TGTGATCCTA GCTACCTGGT ATGTTGAGGC AGGAGAATCG CTTGAACCCA GGAGGCGGAG 960 GTTGCAGCGA GCTGAGATTT 980
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