| Tag | Content |
|---|
EnhancerAtlas ID | HS180-46915 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr8:27975410-27976950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr8:27976157-27976168 | CTGAGTCACCC | - | 6.02 | | IRF1 | MA0050.2 | chr8:27976675-27976696 | TTTTACTTTCTCTTTTGGTCA | + | 6.26 | | JUNB | MA0490.1 | chr8:27976157-27976168 | CTGAGTCACCC | - | 6.02 | | KLF16 | MA0741.1 | chr8:27976395-27976406 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr8:27976395-27976405 | GCCCCGCCCC | + | 6.02 | | SP3 | MA0746.2 | chr8:27976394-27976407 | CGCCCCGCCCCCC | + | 6.11 |
|
| | 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 |
| GH08I028116 | chr8 | 27973625 | 27977015 |
|
Enhancer Sequence | CAAGTGTTGG CATAATTGTG AAATAAAAAG CAGCCCAGAG AAGTTGTGGT TTTGACATAA 60
TGTGGCCCTC GGAAATGTTT GGATTTGACC TTGCCCTTCT CTCTCATCCT GCCCAGAGTC 120
TATGAGTGAA AACTGGTTGG TTTGCACAGC GTAGCCCACT GCTCTTAGAT GTAAGGTGAT 180
GAACTTCATG TTTATTTTAC TTTTGTTTTT GCTTGCTGAC TACATAGATG TAAACTGACT 240
TTCATTAGCT TAGCAGGGTT TTTTAAAGAT TAATTTTAAA TTAGGTTAAA AATGATGTAT 300
TGTGACCTAT GAGTCAGCAA GCAGCATTTA AGGTTAATAG TCTGTTCACG TTAGGGTCAA 360
GTTTTACTGC TGTGTTGGCT CAGGTGTCCC TGCTATGTTT TCATATGTTG AACCTGATTA 420
AAGTTTTGCT TCTTAAAAGA ATAGGAGTTA AGGTAAAGAA AAGCCCCAGC AAGCAGAGCC 480
TGGTTATTAT TTATGGCAAG CTAGTAGCAA GCAGTGTGTT ATATATATTC TCGTGGATGG 540
ATAAATTGGA AAGTTGAGTG AACAGAGAGT TCAAGGACAA AACAGGTATG GCTTTTGTGA 600
AGGCTCATTA AATCAAGCAA AGTGCTAATC ACTCAGTACT ATCAGCTGGA CTGAGATTCT 660
TCAGTAGTCT CCAGAGAGCA ACAATTACTG GTGACTGTCA TCGTGTAACA ATCAGGCTCT 720
GGAGATGAAA AAGACCGGTA GTGGGATCTG AGTCACCCAT TCACTAGAAT GCAAATGTTG 780
CCAAATAACT CCAACAACCT TTTAAAATAG TTTTATTCCT TTTTAATCAG CTTTGCCCAG 840
AAGCAGTTTT ACATTCAATC TTTAATGCTC CTTGGCTGTT TTCACAAGAT GCAATTTAAA 900
GGGTAGTTAC CCATTAAAAA GTGAGTGAGT CATACTTTCT CCCTGTGGAA TTTTAAATTC 960
ATTTCCCGTT CCTTCCTCTT CCCCCGCCCC GCCCCCCACG CCCCATTAAT GACTTTAGAT 1020
CCTCCAACTA TGTTCTTACC TGTCTGAGAA AAGCTGAAGT GCTAGGTAAT GCTAGGTACC 1080
AGGCCCAGAA GACAATTTCG TAGACTTGCA CAGCTGCAAC GGAAGCAAAA GGAACCTACA 1140
GAGACCTGAG AGTGAGTGAC TGTGGCCCTG CTGCCCTGGG CGTCATTTCT GGCAGGCCTC 1200
AGGACCTTCT GCATTTCTGG GCTTTGACGC TGACACTGCT TATCTCTCAC TTTTTCTATT 1260
GACCATTTTA CTTTCTCTTT TGGTCACCCA GATTTCCATA CATGGTGACC AGGATCCTTA 1320
ACATTGGCCA GAGAACATAG GATACAATCT TAGTCACTTT AAGAGAGTTG ATATGGTTTT 1380
TCTTTCAGCA TTTTATTTGA AACAAAAATT AAACAGTTTT TAGTGAGCAT CCACATACCC 1440
ATCACCTAGA TTCTACGATA CTTGCTTTAT CACATATCTG TCAGTTCCAC TATCCATTCA 1500
TCAGTGTCTC TCGCGTGTGC TTGCGCTGTC TTTTTTGATG 1540
|
