Tag | Content |
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EnhancerAtlas ID | HS048-01150 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:43742360-43743770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr1:43742607-43742622 | TGGACTTTGTCCTCA | - | 6.48 | Hnf4a | MA0114.3 | chr1:43742605-43742621 | TTTGGACTTTGTCCTC | - | 6.76 | Nr2f6(var.2) | MA0728.1 | chr1:43743720-43743735 | GAGGTCAGAAGGTCA | + | 7.52 | RARA | MA0729.1 | chr1:43743720-43743738 | GAGGTCAGAAGGTCAAGA | + | 7.51 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_29457 | chr1:43742153-43744096 | Fetal_Intestine_Large | SE_31961 | chr1:43741526-43743587 | Gastric |
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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 |
GH01I043276 | chr1 | 43741976 | 43743274 |
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Enhancer Sequence | CTCAGTGACA CTGCCTTTTC CTGGTTGGCT CCTGCTCCTA CCGTGACTCT GAAGTTCTCT 60 CCACCCTCTT CACCACCCCC AACCCCCACA TCCTCCCACC CCAAACACCA CTCTCAGCAA 120 AAGACAGCCT CCTCTCTTCA TGAGAAGGCG AGAGCCCGTG ACAGGAGCCC CTCACCACGG 180 CCCCCACCAA ATCTATCCTC ACTTACTCCT ACTTGTCCAA TGGCCTTGGC AGCCCAGCAG 240 AGGAATTTGG ACTTTGTCCT CAGGACACTG GAAAACATGG AAAGACTTTC GCCAGGGGAG 300 TAGGGTACTG TGGCCAGAAT AGGATTTGGG ACTTGCTGGC TGCGGTGTGG AGCCAGGGAT 360 TGGCCTTAGA AGAAAAAGAA TGAGAAGAAA TGGCCAAACA GCCCGTCTCG GCTGGCCACT 420 GAGGGACGAG AAGAAGTTGG CCCAGCTAGA GAGGTTAGGA AGAGTATCCC AGAAAGAAGG 480 AATAGCACAA AGAAGGGTCC AGACCTGGAA ATCTAAACTG GCATTGGATG AAGGAAAAAT 540 CCAAAACAAG GGCTGATGGA GAGACAGCAC AGCCTTGTCT GGACCTAGAG GCTCCCATCG 600 GTGGCAGTGA GGTGGAGAGA GGAGCTTGAC ACATGTCCCT CCTGGGTTTA ACATTCAAAC 660 TCTAGGTTCT CAGCCATGTC CCTTCATATC TGAGACTGGA AGAATATGCT CTAGAAACTG 720 CCAAATCTGG TCCAGTCCAG GTGGTCCTCA CATCACATCC AGTCACATCT CACAGGAGAC 780 CTTGGGCCTC TGGACACTCA GGTCTCAGAC CTTGGAGGAG CTTCCTCCAG GCCCCAAGGG 840 ACCTGCACAT GCCCCGTCAT ACTCAGCTCA TGCAGGAGCA CAAGGACAGG GGCTGCCTTC 900 CTGCCTTTTG CAGGGGACCT GTGAGACTCC CCTGGGCATA GCCCTGGCAG CCACCCCAGA 960 TACCTGGAGG GCAATAGAAG CTGAGGGCCA GGCCCGGCCA GAGATGGGAC ACACCAGCTC 1020 TACCCTCATG ACCTGCTCTC CCAAAACTGG ACCTTGTACC CTGGGACTTC TCAGCCGCTA 1080 TTCACTGTAG AGGGTAAAGG TGGGAGGACC CAGCCCAGGC AAGATGAGAG TCCAACAGCC 1140 GAGACAGTCC TTCTCTGAGT CTATTTCATC GTTACTTCAA GGTGAGATAA TGGTGTTATT 1200 GCGGAGTGGG CAAATTGCAG TGAACTTGTT TGAGCCTCAT CTTCTCAATC TATAACATGG 1260 ATTAAGCAGG GCTGTTGTAA GAAAATGCTA GAACAGCCTG GTGTGATGGC TCACGCCTGT 1320 AATCCCAGCA CTTTGGGAGG TCGAGGTGGG CGGATCACTT GAGGTCAGAA GGTCAAGACC 1380 AGCCTGGCCA ACATGGTGAA ACCCTGTCTC 1410
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