| Tag | Content |
|---|
EnhancerAtlas ID | HS048-33182 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr7:141860-143370 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr7:142476-142492 | GGGGTCAGAGTCCACA | + | 6.58 | | MAFK | MA0496.2 | chr7:142706-142725 | AATTCCTGACTCTGCAATC | - | 6.12 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 142200 | 142376 | | chr7 | 142585 | 142695 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I000140 | chr7 | 140601 | 144400 |
|
Enhancer Sequence | TGTGTTCCTG TCGGGGGTGA GCCTTCCCCG TTGGAGGTGG GTTTCCGAGG TTGTGTTCCT 60
GTCGGGGATG AGCCTTCCCT ATTGGACATA TGGGTTTCTG AGGTTGTCTT CCTGTCGGGG 120
GTGAGCCTTC CCCGTTGGAA GTGGGTTTCT GAGGTTGTGT TCCTGTCGGG GGCGAGCCTT 180
CCCCATTGGA AGTGTGTTTC TGAGATTGTG TTCCTGTCGG GGATGAGCCT TCCCCATTGG 240
ACGTGGGTTT CTGAGGTTGT CTTCCTGTTG GGGGTGAGCC TTCCCCATTG GAAGTGGGTT 300
TCTGAGGTTG TGTTCCTGTC GGGGGCGAGC CTTCCCTGTT GGAAGTGGGT TTCTGAAGTT 360
TGCTGTTGGA AGCAGAGCTT GCGTCCATGC TCACAGCAGC ACCAGCCGCA ATCAGTCACT 420
GAGGTCTGTG CTGGGTGTGG AAGATGAGAG TGGTACCACA TGTTCCTCAA TCTGGACTAG 480
AGGTTTGTCT GTGATTAGCG GAGACTGGCC TGCCAAGAGC CAAGGGCGCT GTGTTTGCAT 540
GTACAGCAGG CGTCTGATAC GGTTCTGGGG CAGACGCCAG CCAGGCCGAG CAGGCAGCCT 600
CCACTGCTCC GTGCATGGGG TCAGAGTCCA CAGCATGGGA CCTGGTCCCT GGGCAGGCCT 660
GACAGACATC TGTGAACCAG GAATGGGCAT ATTCCAGGAG GTCTGGCACA AAGCAAAGTC 720
ATTGTAGACT TTGGCAATTG CATTTGTTCC AGATAATACA TTTTCTTAGG ACCTAAGGCC 780
TCAGAACTTA AAATGAATGT TGTAAAGTTT GAAGCCAAAA CAAAATGCAG ACAGGCTGTA 840
CCCAGCAATT CCTGACTCTG CAATCTGGGC CTAATTCAAG TACTCATCTC CATGGCCTGC 900
CAAAACCCTC CCACCGGAGC TCACCCTGTG GTCCAGTGCT CAGCACCATT CATACCTATG 960
TTCGGGGACA GAAGCCACTC TGGGGACTAG GAAGAAAACA CGTAAAGGAA TTGAGCTTAA 1020
AATAAAAAGA AATTCGGTAT ATTTCATACC CACTAGCAAT ATGCCTTTAG AAAGAGACAG 1080
GCTGGCAACT GCACGTTGGG AAGGACGCAC AGTGACTAGA ACTCTCGTTC CCTACTGCTG 1140
GGAGTGCAAA ACGGAACAGC CACTCTCCCG ACTGCCCAGC GACCACACTC CCGGGTGTTT 1200
ACCCAAGAGA AATAAAAATC GTGTCTGTAA AAGAATGTCT ATCAGCCTTA TTGATAACGT 1260
CTCCAAACCC TGATTACATC AAGTGTCCGA CCGCAGGAGG ACGGACGAGA ACGGGTGGCC 1320
CTTCACAGAA CAGGCTAATT CTCAGCATGT GGGAGCACTC GTGCGTGGAA GGCCAGGCGT 1380
GTGACACGTG TGAGCATAGC GTGGGCAGGA CGCACGTGAG GGCAGTGGCG GCTTCAAGCA 1440
CAAATCCTAG GGACTGGGTG GGTCCTTGGA GCAGCAGGCC TGGGTGAGCC TTAGTGGACT 1500
CCTCTGTGGC 1510
|
