| Tag | Content |
|---|
EnhancerAtlas ID | HS050-14880 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:6197540-6198870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr12:6198441-6198452 | TCTGATTGGCT | - | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27167 | chr12:6197847-6198954 | Esophagus | | SE_37940 | chr12:6196664-6208010 | HUVEC |
|
| | 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 |
| GH12I006088 | chr12 | 6197275 | 6199142 |
|
Enhancer Sequence | AGGCTGAGGC GGGAGAATGG CGTGAACCCG GGAGGCGGAG CTTGCAGTGA GCCAAGATCG 60
CACTACTGCA CTCCAGCCTG GGCGACAGAG CGAGACTCTG TCTAAAAAAA AAAAAAAAGC 120
GAGAGAGAGA GAGAGAAAGG GGTGCCTTTT TCTAATTAGC AAAAGCATGC TATGAGCTGG 180
ATGCAGCCCA AGCCCAGCCC CCCGGAGCCT TGGGCTTCCT GTTGCAGACA GGACTACAGG 240
ACAAAGCCAA GATCCCTTTG TAAGGTTCAG TCCTTGCTGG CCTTCCCCAG TCTGATCGAA 300
TTTTTTTAAA GTGATCTAAG GGTCTTTCTT TCTCAAAGGT ACACTTTGTG ATAGTTACCT 360
GCAGATGAAC ATCAATTATC TGAATGTTCA TAGCTTGGGG CTCCAAACTC CAACCATCTT 420
GCCTTCAGTT TGAAAAGCTG AAAAAACTGC AAATTTGCAT GCAATCAAAC AAGGCCATTA 480
TCAGTCCCAG TGGAGACAGG CATTGGGTTT TGTTGGCATA ACAAGGAAAC ATTCATTCCC 540
TAGGTATAAC TAACAAGTAA TATGACCTGG CTCTCAGAAT GAGCTGACTC CTTGCTATGC 600
CCTAGAAAGA CAGAAAGCAC CAGAGGGTTG GGGAAGTAGA TTCTGGAGGC TGTCAAGGAA 660
AGTTTCAAGG TCAGTGTGAA CTCCCACACA AAACACTCTG CCACCCCGAA CGGCCCTTGG 720
AGCCACAACA GCAGACACTC ATAAATGATG CGGCATTTAC CAGACCGGAC TTCTGAACCT 780
GGGGGCCCTG CGGGACTACA CAGGCTGTGA ACAATTCAAA AGGCCATATT AATCACCTCT 840
TGGGAGACGA GTCATTGTGC TTCCGAGCCA GTGAAAAAAC CTCGGTTGTG GGCAAACACT 900
ATCTGATTGG CTGAGGACAA AGCAGTCTTC TCTTCTCAGG TAAACAACCT GAAACCGGGA 960
GTTCTGAGCT GGGAGGAGCT TGTGCCTCTG GGAGGTCTCA CGTGTTTGTG GCCTCAGCCC 1020
AACACGAAGA ACCTGGTACC CAGTTTTTTC AGCTGTTCCC AGGACACTGG TTAGTAAGGA 1080
CTTTAATGCA CCCAGGAGAC AAAGCGAGTA GCTAGGGTAC AGCTGGAGCC TCAGAAAGGT 1140
GCCCCGGGAG GCAAACAAGG CTTCTCTTGC ATTCTCCCTC CCCTTTGTCT CCAGGAGACA 1200
AACCTCCCAG TCTCCCTCCT CAACCCGACC TCAGGATCAG GTTCTCCACT TGAGAATCCT 1260
GTCTTTACCT CCCACTCAGT ATGGATAAAT GAGATCATTC CTTTGTATTC CGAGGGTAGG 1320
GAACATTTGT 1330
|
