| Tag | Content |
|---|
EnhancerAtlas ID | HS050-40563 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:237855140-237856250 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr2:237855337-237855352 | TCTGACCTTGAACCC | - | 6.7 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTTGCAAAC AACAGACGTA GACTCTGGCT AATTGAAGCA AAATAGTATT ATATAGAAAA 60
AAATATAGAA TCTGTCACAA AATAGAAAGA CAGCTAAGAA CCAAGCAGCT GGAGGGGGCT 120
CTGGGTGCAA GAACTACTGT GTAGCCAGGT GGTCTCTTCA GGGCTCAGTT CTCACAGCAA 180
ACAAGCCCCA GCCAATTTCT GACCTTGAAC CCCTCAGTTT GATGTTCAAA TGTTCAAGAG 240
AATCTAATTG GTCTGGTCTG GGCCCTGTTC CCAGTTTTGG ATGTTGGATG CATTCAGAGT 300
GGTGGTGGAA ATGGGAGACG GTGGGTCCCT AAAGGAACAT CAAGGTCCTA TTACTAGGAG 360
AAGTGGGAAG GGATGCCAGG CAGGTAGAAG CACATATGTC CATCGGAAGG CCTCAGACAG 420
GACACAGGCA CAGTGAGAAA CCAGAGAACA TTCCCACGGA GCAAGAACAC TTCTGAATGT 480
AACTACAGTC CTGTCTGTTG AATGTTACAA GCCCAGATTG ATAAGCAAAT TTCCCTGGGG 540
TCAGCTGGTG CTAACCCCAC ATGGCAGGAT GGAGCAAGGC TGATGGATGT TGTTTATGGA 600
AACTGACCAC GTGGTAATCT TGCAGCCACA CTCCAGCTAT TGTCCCGCAG GATATGAGAT 660
AGAATTCACA TGCTTCAGGA AGGGTGAGTG TTAAACAGTG TGTCATTTCA GCAGGGAATG 720
AGATAGAGGA AGAATGGGAT TTCTAACTGA AATTCCACAG CTCAGCCTCT CTTTTCAAAA 780
CCCAGCAAGC CCAAGACCAC CTTTAAGCTG GAGCCCAGAA GTGGGCCACC TAGTTCAGGT 840
GAGACTAGAC CTGGAGTGAT GCCTGCATTC TGGCCCTGGG TCTGCCACGA CTCAGCTTAT 900
GTTTTTAGAT CATCAATTCA TCTCCTTGGG CCTCATGTGC TCATCTTGAA AACGAGGCTA 960
GTTGTTAAGG TAACGTTCCT TGTCATACCC TTTTCTGAAA CTACAGCCAA AAGGCCCAAG 1020
CTGTACCATG TGCAAAGCTA TTTGTGACTC CATCTGGGGT TTTATCACAA TGTACACTGA 1080
TCATTTCACT GTGTGTGTTT CCCCAGTGGT 1110
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