Tag | Content |
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EnhancerAtlas ID | HS048-06652 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr11:59497970-59498940 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr11:59498841-59498856 | GGAGTCCAAAGGCCA | + | 6.74 |
| | 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 |
GH11I059730 | chr11 | 59498349 | 59499633 |
| Enhancer Sequence | TGCAGTGAGC TGAGATCGCA CCGTTGCACT CCAGCTGGGG TGACAGGGTG AGACTCCGTC 60 TCAAAAGAAA CAAAATAAAA CAAAACAAAA AACAAAAACA AAAACAAAAC AAAAGTTTGA 120 CATATGAAAA TGCATATTTC AGGGGTAAAT TATGGGCAAT TAGACAAAGG AAGTCCATAA 180 GAGCTTTCTG AGTTTCATAA TCATTAACTA CATTTTGAAG TCTTGCATTG CAATAAGTAG 240 CTGCTTTTTT TTTCTTTTAG GACATGGCTC TTCCTGGAGA ATATGCTCGT ATTCATTTTC 300 TATGTGGTGC TGCTGTTTCA GAAATTCTTC TGTGATTCTA TACACATGGA CATGAGCATT 360 CCCTATTAAA TTTTTTCATC TTCTGTGCCA TCCATCTATA TTGTTTTGGG CATGTGGAAA 420 TCCATACATT TATATGCAGA CCATAAATTT GGCAGAAACA ATACTGGTGA TCAAACAGCA 480 ACACCATTGT GTGTCTTCTT ATCTTAGCTT GCACATAATT ATTTTTGAAC CAATCAGTAA 540 CTTCACTGGC TTCTTCAGGC AAATGCAACT TTAATTTGTT AAAAGTTTCT GGCATGTCAT 600 CAGCTGAAAG GAATGCCAAT GCAGGCAAAT TATCCATTCT CACACTGAAG TTGTTGTCCT 660 TGTCATATCA TGTGGCCAAT TCACTCATCT GAATTTTTCA CCAAATGCAT TGGGATGAAT 720 TTTTTAAAAA AGCTTTTTAT TGGTAATACT TTGAAATTCA TTTTTAGGAG TCTTGATTGC 780 ACCTAATTCC AAATCTGTCA TAACTAGGGA GACTGATGGT GTAACTCTGA GTCCGAGGCT 840 GACAGGAACC TGGGAGCTGC TAGTGAGTCC CGGAGTCCAA AGGCCACTGG CCTGGAGTTC 900 TGATGTCTAA GGCATCTGAA GAAAAGTGTG TCCCAGATCT CAGAGAGAGT CAGTTTGCTT 960 CTGTTTTTGT 970
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