Tag | Content |
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EnhancerAtlas ID | HS180-47190 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr8:48265270-48266700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr8:48266326-48266343 | AAGAACACAGTGTTCTG | - | 6.13 | Ar | MA0007.3 | chr8:48266326-48266343 | AAGAACACAGTGTTCTG | + | 6.54 | NR3C1 | MA0113.3 | chr8:48266326-48266343 | AAGAACACAGTGTTCTG | - | 6.23 | NR3C1 | MA0113.3 | chr8:48266326-48266343 | AAGAACACAGTGTTCTG | + | 6.54 | NR3C2 | MA0727.1 | chr8:48266326-48266343 | AAGAACACAGTGTTCTG | - | 6.28 | NR3C2 | MA0727.1 | chr8:48266326-48266343 | AAGAACACAGTGTTCTG | + | 6.53 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_09525 | chr8:48263813-48269233 | CD14 | SE_27599 | chr8:48264868-48266626 | Esophagus | SE_36331 | chr8:48264477-48272342 | HMEC | SE_64835 | chr8:48264643-48272634 | NHEK |
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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 |
GH08I047351 | chr8 | 48264317 | 48272499 |
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Enhancer Sequence | TGGGAGACGC AAAATTTAAA GTAGGGGAAA AGGAGGATGG CAAAAACTAA GTAAAGTAAC 60 TTGAAAAGTT ATTCTTTCTG CCAGGCGTGG TGGCTCACGC CTGTAATCTC AATGCTTTGG 120 TAGGCCGAGT CGATGAGGTT GAGAGATCGA GACCATCCTG GCCAACGTGG TGAAACCCCA 180 TCTCTACTAA AAATACAAAA ATTAGCTGGG CGTGGTGGCA TGCACTTGTA GTCCCAGCTA 240 CTTGGGAGGC TGAGGCAGGA GAATTGCTTG AACCCAGGAG GCAAAGGTTG CAGTGAGCCA 300 AGATCATGCC ACTGCACTCC AGCCAGGCGA CAGAGCGGGA CTCTATCTCA AAAAAAAAAA 360 AAAAAAAAAA AAGTTATTCT TTCCAAATAT GATACAATTT TGTTCAACTT AATTTTGTTA 420 AATTTTTATT CAAAAAGTTA AGTTCTAAAT AGCATCAAAC ATGGTGGGAG TCAAAATAAT 480 TAAAATCGTA TTTTTTCTGA AAGTGTGTAG ACTGCCTGCA TACTTATATA TACGCCAGAT 540 TGTATTTTAC TTACCTTCTC ATTTGCATCT TACCCTTGTG GCCGAATTAG CAGGACCTGT 600 GTGAGAATGA CATAACTTCA CCGCCTCTTA CCTGCTCCAG CTGCAACGCG TGAGAGTGCT 660 GAACTGTGGC CTAGATTTTT CTCTAGGGCT TTCCACGGAA GTGAGTCAAC ACATTGTTTC 720 TGGCTTTTCT TGCTGTCCCT CCCTAATATG CAAGCTTAGG TTGCTTTGGA ATTTTCCAGG 780 TACAGTGTTG GAGAAGTTGT AACACAGGAG GAGGCCAGAG CGTAGGTTTA GTGTGGTGGG 840 GAGAGGGTTG GAGCAATTGT TCAAGGGAAG ATTGAAAGTG ACCAAAATGG CATGAGGGTA 900 AAAATGTTAC CTGAATTAAA TATGTACCAA ACACTGAAAA TCCCTTATTA TATTTTAGTA 960 TCTTTTATCA TTGTATTTTA AAATTGATTT AAATCTATAC TGAGATTTTT TTTTTTTTTT 1020 TAGTGTGGAT TTCAACACAT TTTTTGTGCT TTTGCCAAGA ACACAGTGTT CTGTTAAGTC 1080 ATTCAGTGAC GAAGATTGCT GGATTGCTGC CAGCCCGGGT CAAGTTCATT CACATAAGTT 1140 TCAGTGTAGA TTCTGACTGA GTGAGGAATG TTCCTCTTGT CTTTGCATGT TAGGTGGGTC 1200 TGGGAAATCA GTTGTTTTAA AACAAGCTTA TTAATACTTT TGTTTTTTTC AGGGTTATGG 1260 GGTTTTTTTG CTTTTAAGGC TTCATATACA GACAACGCTT TGATACTAGT ATCACATTCT 1320 TGTCTATTTA CTGATTTTCC ATGCCTGATT TGGTGAAATA ACAGCTCTCC TAACCATACC 1380 AGATTAGAAT CTACCGTATA ACGTATTGAC TCTGCTGTAT CATTTTAAGG 1430
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