| Tag | Content |
|---|
EnhancerAtlas ID | HS050-34861 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:33290-34390 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ONECUT1 | MA0679.1 | chr2:34113-34127 | CTAAAATCGATATT | + | 6.33 | | ONECUT2 | MA0756.1 | chr2:34113-34127 | CTAAAATCGATATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27296 | chr2:32558-37040 | Esophagus | | SE_39727 | chr2:32373-35071 | Jurkat | | SE_66662 | chr2:32373-35071 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 33437 | 34204 | | chr2 | 33488 | 34349 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I000033 | chr2 | 33007 | 39505 |
|
Enhancer Sequence | ATTGAATCCT TAGGGGGCTA ATAGGGTTAG AATAATAATT ACTACCATGG ATTGGGTGCC 60
TCCTTTGTGC TCAGTGCTTT TAAATACGTC TCTATCCTCC AGTCTTCATG GCCACCTTCT 120
AACAGATGAG AAAACTGAGT GGCGTTTAAT GTGCTCCAGG TCAACAGCCC CTCAGCGCAT 180
TACTCTGACC TGCTGTGGTA ATTCCATGAT CCTAAAATGT TTGGCTTCTA TGAGCCTCGA 240
CTTCAGTGTG TACCCACAGT ACTTTGTACA CAGATACTGA CACTCCTTTT CAGAGTTCCA 300
AGTTTAATCT CTGTTGTAAA TGCATATTTG CTAGAAAATG TTCTTCCTTG GAGAAGGACC 360
TGTAACTCTC TGACAGCGTT CCTGACACTA CACCAGGAAC GCTGGCCATA GTGACAACGT 420
CGATGTACCC TGTGATAGGG GTTAGCATTA GGTGTGTAAT GCTGAGTAAT GCAGGCAGGG 480
AGGCAACAAC TTCCTGTTAC CTTCAAGCTA GAATTGCTCA GTCAACCCAA AGCCACCGGG 540
AAAAGGTGAG TAACGCTTCC TTCCTGCCTC TGCCTGCACG GTCAAATTGT TGACAGTTGG 600
CTCAGTTTCT CTTCTCACCT GTAAAAGGAT AATATTTGTG TAGACTTGGA ACACATGCAA 660
GAATCTGCAA GTAGATATTT GGAATGTGCA TGTCTTGGCC TTTTCTTCCA CTGTTGCTGG 720
AAAGAAACCC AAAGAACTTA AGCTGTGCTG AACTTTCCGG TACTTCAAAG TAAACTTAAA 780
GGATTTCCTG TTCTTTTTAC AACTGTGGTC ATTTCCCATT TACCTAAAAT CGATATTAGC 840
CACCACTGAA ATAATCATAG TTCTGCTAGA CTTCTCTGAG GTGAGCTAGA AGGTCTTGGA 900
CTTCGAATCC AGACTTAGGA TTCCATGATA TACAAGAGGG GGTTGTACTT GAAATTTACA 960
ACTCTGTAGT GGAACTTGTG CCCCAGCAAA TGGGCCATCA GCCAGTTCAA CAGGTTGCCG 1020
CAGTGTGGAC CTAGTCAGCA CTGCCCTGAG CTCTCTGGAA TAGTTTGCTT TCCCTCAGAT 1080
TTTCTCTTTA TTGCTATTCT 1100
|
