| Tag | Content |
|---|
EnhancerAtlas ID | HS050-66726 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr8:98993380-98994730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr8:98993765-98993780 | AGCTGAGTCATGGTG | - | 6.61 | | ZNF263 | MA0528.1 | chr8:98994380-98994401 | GGAGGAGGGAGACAAGAGGAA | + | 6.65 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_56330 | chr8:98990845-98998258 | u87 |
|
| | 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 |
| GH08I097980 | chr8 | 98992264 | 98994643 |
|
Enhancer Sequence | CCAGCCTGGA GGACACAGTA AGACCTTGTC TTAAAAAAAA AAAAAGGCTA AAAAGGGATG 60
ATGTGGGTTT CAAAGACTTT ATTTATTATC ATTATGTTTT TTTAGAAATA GGATCTTACT 120
CTGTCACCCA TGCTGGAATG CAGTGGTGCA ATCCTAGCTC ATTGCAGCTT CCAACTCCTG 180
GGCTCAAGCA ATCCTCCCAC CTCAGCCTCC CAAAGTGCTG GAATTATGGT CATCATGAGC 240
CACCACACCT GGCCTCCAAA ACTCTAAAAA AATGAGTATT TAACTGTGCA TATACCACGT 300
GCCTGGGCTA CATTTAAAGG TGCAAAAAAC ATTCAAGATT TCCACTGCAA GCTGGTGAGG 360
GACCTTAGCC ATAGCCACAC TGAGTAGCTG AGTCATGGTG CCAGGAGTTA TGTGACCAAG 420
GGCCTACAGT GTGATGCAGC CAGGACCACA GCAGGAGTTA GAGGAAGGAG ACCAGTTAGA 480
CCAGAACAGG TGAGATGCTG CCTTGCAGGG ATGAGGACTG GAGAAAAACA CATATCCTAG 540
CCAGTCTCCT ACCTGCCTCT CCAGACTGCA CACACTGGCT GGGGTCACCT GATTTCCACC 600
CCAGCACCAG CCCTAGTTCC CAGAGTGGCA CCATCTTCCC CACCCTGTGG CTCAGCATGC 660
CTCCTGTCCC AGATCCCCAG CCCAGGGTGG TGCAGGCAAG GAGGGTGTTG GAGCCCTGGA 720
ATCAGACCCT GGAAGTAGAT ACCGCAGCAT AGTGGGACTG GGAGAGGAGG TTTGGCTAGG 780
AGCCACGGGA GGGGCTGATC CAGCTGTGAG GTCTCACCAG CTAGGCAGCG AGCCCAGCAG 840
TGCAGTTGTC AGAATCAAGA TCCAGAAGTG GGCCGCCCCA ATGCGTGTGC AGGGAAGAGT 900
GCTGGGAGAC TGGAGGGTTC GTGCAGGCAG CCTCAGGGCA GTACATCCCT TAGAAGAGCC 960
CTCTTCCCAC CATGCTTGGG GTGGGCAGGA GCCAGACCCA GGAGGAGGGA GACAAGAGGA 1020
AGAAAGGAGA CAGAGTACTT GGAAAGCTAA GAGTAGAAAA TAAGGCAAAA GCCCAGTCGT 1080
AAGAATGAAA CACTCAGGAG TGCTCCAGAT CTGTGGCAGG GACAAGAACT GAGAAATAGA 1140
GACTAGTTAA AATTACAGAA ACAGGATAGA GGCAGAAGCT CAGAACCGAA GCAGCCACCC 1200
TGTTTTAGTG AGTACCAAGG CCTCCCACCA GCTTCCAGCC AAGTCGGCCT GGTTACTGCT 1260
GTGATGTTGA AAGATTTTTT TTTAAAATTC TACTTCTTAT ACACTTGCAA AAAATGAAAG 1320
AAACTCAGTT TCTCAAATTT CAGCCTATAT 1350
|
