Tag | Content |
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EnhancerAtlas ID | HS048-21008 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:110315460-110316890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arid3b | MA0601.1 | chr2:110316129-110316140 | ATAATTAATAT | - | 6.02 | HNF1A | MA0046.2 | chr2:110316061-110316076 | GGTTAATCTTTAATT | - | 6.52 | NFE2L1 | MA0089.2 | chr2:110316237-110316252 | CCATGACTCAGCATA | + | 7.22 | Nfe2l2 | MA0150.2 | chr2:110316235-110316250 | CACCATGACTCAGCA | + | 8.73 | Nr2f6(var.2) | MA0728.1 | chr2:110316681-110316696 | TGAACTCCTGACCTC | - | 6.22 | POU4F2 | MA0683.1 | chr2:110315672-110315688 | ATGAATATTTAATGCC | + | 6.51 |
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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 |
GH02I109557 | chr2 | 110315365 | 110317471 |
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Enhancer Sequence | TCATCCAGGC TGGATCATCC TGCCTCTACC ACCCAAGTAG CTGGGACTAT ATGAGCATGC 60 CACCACAGCT GGTTAATTTC TGTATTCTTT GTAGAGACAG AGTTTTGCCA TGTTACCTAG 120 GCTGGTCTCA AACTCCAAAG CTTAAGTGAT CCACCTTTCT GGCCTCCCAT AGTGTTGGGA 180 TTACAGGCGT GAACGACTGC ACCTGGCCTG ACATGAATAT TTAATGCCAA CATACTACTG 240 TTGTTGCAAA TCTCACTGAT TTAAAGTTGA AAACTAAAGA GAAAGAAAGA AAAAAATCTC 300 AGATGCTCAT GTCATCAAGA AAAGTCCTTT CCTTCAATTG GGACATGTTT GTGTTTCAAG 360 TACAGTTCCG ATAAGCCTAG TGAACTTTTT CCAAGTCTAC TATAGACTAC CTGAAGAACT 420 ATTTAGTTCT TGAGAATTCC AAAGACATGA AGTTTTACTA AAATTACGTC AAATACTTAA 480 ACAACTCTAA ACTACTAAGC ATACATCTTC CTTTCAAAGC TACAGGTCCC ACAATACTTC 540 AATGACAGTG ATTTTGTGCT AAAAAGTTAA AGGTGATTAA CTGTGGGAAA GAGATTAGTT 600 AGGTTAATCT TTAATTATTA AACTTGGGGA TTTAAAGAGT TTTATAAAGG CATGTTTCCA 660 ATGGTTGAAA TAATTAATAT AAAATGTTAA GATCAGTTAA TTAAACTATG ACTATAGTGC 720 TATTTACGTG GGCCTCGTGA CAAGCCTGCG ATTGGTGCTG GTAGATTAGG ATACCCACCA 780 TGACTCAGCA TACCCATTCA ATAAAGTGTA AGTGGAAAAA CAAACGGAAG TTCTGGCAAC 840 AAAGAGGGCC AGGAAGTACA GTCACATAAA GGTCACCCAA CAGGTTTGCG TAACTTGTCT 900 TTACTGCTAG ATAGATATAA TACTGAGGGA CAGATTTTAC ATGCCAACCA AATTACAACA 960 ACTACCAAAT TAAATAGGAA AAGACTCCCG AGAAAACAGA TATAAATTCT TTTTTTTTTT 1020 GAGATGGAGT CTCGCTCTGT TGCCCAGGCT GGAGTGCAGT GGTGCGATCT CAGCTCACTG 1080 CAGCCTCCAC CTCCTGGGTT CAAGCAATTC TCCTGCCTCA GCCTCCCACA TAGCTGGGCT 1140 TATAGGTGTC CGCCACCACA CCCGGCTAAT TTTTGTATTT TTAGTACAGA CAGGGTTTCA 1200 CCATGTTGGC CAGGCTGGTC TTGAACTCCT GACCTCAGGT GATCCACCCA CCTTGGCCTC 1260 CCAAAGTACT GAAATTACAG GCATAAGCCA CCACGCCTGG CCAGATATAA CTTCTTGAAA 1320 CTATAAAAAA TAAAAGCTTC CTAATACATC AGACTATAAT GAGCTACAAA AGCCTTATCA 1380 AATCATTTAA TCACATATGA CAAAGAACCA GAAGAGACAT TTTGCCTCAA 1430
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