| Tag | Content |
|---|
EnhancerAtlas ID | HS050-66736 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr8:99190920-99192310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr8:99191212-99191226 | TGCCTTTGATGTCA | - | 6.22 | | ZEB1 | MA0103.3 | chr8:99192094-99192105 | GCGCAGGTGGG | - | 6.62 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_37626 | chr8:99190338-99192697 | HSMMtube | | SE_46054 | chr8:99190358-99192707 | Osteoblasts | | SE_52165 | chr8:99190984-99192304 | Skeletal_Muscle_Myoblast | | SE_63956 | chr8:99190984-99192403 | HSMM |
|
| | 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 |
| GH08I098177 | chr8 | 99190052 | 99192672 |
|
Enhancer Sequence | ATGAACTCCA CCCTTCTCAT GTGATACAGA AAGGCCTGGA TTCTGGTGGG TGCAGAAGGT 60
GATGAGAGCT GTCAACACTA GTAGGATCTG TGGACCCCGG GCCAGGTGGC CAAATGCCTA 120
GGATGCTCAC ATTTGGACAC TGGTGTCACT GCTTTCTGAG ATCCCTTCAC ACTCATCTCC 180
TCTGGTCACT TCTCATGTCA CCACGTTTGG TTTGGCAACT CTTGCGGGTG GCTGCCAGGC 240
CCTCTTCTCC TCTGCAGGCC CCTTCTGCTT CTCCAGCGCT GACCAGAGTT TTTGCCTTTG 300
ATGTCACTTC AATGTAATGT TCACCACCTG AGTCACGTAG TAGGTGCTTG GCCACTTCTG 360
GAGACAGCCT GAGACAAATG TTGCGTGACA ATCTTAGACA CCTTCGAGGG GTGTCTTCCT 420
GTGTTTGCAC TGTGCACGTT ACACAGTTGT GTGCATGCCA GCACCGACAA AGCCCCCATG 480
TCCCTTTGCT GAGCAGTTTT CAAGCAGGGC TGTTGTCCTT GCTGCTCTGA CATGGTCTCC 540
TTGCTATTGT TTTCATCTTT ATCCTTCAGA CCTCAGCTGA GATAAATCTT CAAGCTCTTC 600
CCCCACCGCC TGAGCGAGCC TATGACTCAT GAAGCCCCAT GCTTGAGAAC AAACAGGCTG 660
TCTCCTCTTC CCCGCCTCTG CCCTCTGTGA CCCAGTGCTC TTTCTCCAGC AATGATGAAC 720
CTTTATTGCA GCGACAGGGC AGGGTTTGGT CCTGGGATGG TGACATTATT AAAAACAGAT 780
TTAGCAATGC TCCAAGTAGT TAGTCCGCCT GCTCTGTAAT GGTTTATCAT AGTCATAAAG 840
CTGACTGTTG GGGTCAGCTG ATCTCTGCTT TTAGACACGA CCACACCTAC GTCATTCCAA 900
TGAGATGGAA TTATCTTTTA TTTGTTGTTA TTTTTTAAAG GCCTCCAGAG AGAGCTTAGA 960
GCTCCCCCTC CTTCAGAAAC CTACTCTGGC GTTACAATGT TGCTGGGGCC ATGTCATTGA 1020
TCTGTGTGTG TGCATGTGTG TGTGTGTGTG CATGCATGTC ATGTGTACAC GCTGGGTTTC 1080
TACAGTGATT TCTGCCCCCA CCACTTGCTC TCTATCCGCC CTTCTTCAGG CACAGGGTCT 1140
GAGACAATCA CAGCAGAGGA GCCTGCAGAC AGCAGCGCAG GTGGGAGCTC ATGGCGTGGG 1200
AAGAGGCTAC ACATTTCGGT GCCTGGATTC CAATCTACCT CCTTCACTGA CTTGCTGTGA 1260
CCCAAGGCAA AGCTGATTAG TCTCCCTGAG CCTCAGTTCC CTCAAGTGTG AAAGTCATAA 1320
TAACTGAATT TTCAGTGCCA CCAGGATTGG AGGTAATATA TGCAAAGTGC CTCGTCCATA 1380
GTAGGTGCCC 1390
|
