| Tag | Content |
|---|
EnhancerAtlas ID | HS048-22000 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:208790690-208792110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox3 | MA0514.1 | chr2:208791952-208791962 | AAAACAAAGG | - | 6.02 | | Tcf12 | MA0521.1 | chr2:208791218-208791229 | AACAGCTGCTG | + | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35788 | chr2:208790046-208792285 | HepG2 |
|
| | 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 |
| GH02I207925 | chr2 | 208790334 | 208792196 |
|
Enhancer Sequence | CTGAGACATC GACAAACTCT GTTCTTAATA TTTAATTACA TGGCCTTGGG GTTAAAACCT 60
CGAATGCCTA GGCCCAGGGA ACCACCATAA ACGAATTAAA TGGGCTGGAG ATGAGAAAAA 120
CAGGGCAGCA ATGTGTTATA TGCCAAGTGG CACTGGGTTT GGGGAGACAA ACTAGAGCAG 180
AAGAAGTTAT GGCAAAGTGG CAAGTCAAGT GTCTAAAGCT GATCTCTGCT ACACAGAATG 240
AGGGAAGTTC TGTGTAATCA GAACTCATTT CCCAAGAGAA ACCAGAAAGC TTCACTTTGT 300
GTGTGCATGA AAACTCCTGA TTTTTTTAAA GTTGGCAACT ATTTCACAAT TTCAAAACTT 360
TGTGGGGCCA TCCCTGTGAG GCCAAACAAA ACATGTCTGC TGGCCAAATC TGGCCTTGAG 420
GTGACACATT CTACCGTGCC TGTGTGTGAC ACATCCTGCT GTTCCTGTGT TCAGCAAGAG 480
CTGAGGCTCT TCCTAGCAGT TCTTAACGTC CCTCCCAGAA ATTTCCCTAA CAGCTGCTGA 540
TCCGGATGTG TCCTGACATT GCCATGTATG CCCAGATTTT CCACAGAGTT CTTCATGCAC 600
CTTCATGTGT GGACACTGTA AATAATTCTT CTCATGAAAA GTTAACTAGA CCTTGAACTA 660
ATTCAGCAGG ACCGCCATCT GGGAGTCCTC AGAAACAGTG AATTGTCAGC ACTGTAAACA 720
TTTTAAGCTT CGGGGAGGAC ACTGACTTTT TCTAAACTAA TCACCCCTGC CAGTCAAGAT 780
GTGCAGTGTG GGTTCAAGAA CAAGGCGTTC ATTTAACAAC AATAACAAAA ACAGTGAGGA 840
TGAATACCGG ACAGCCATCA TAATGAAAGG CCTAAAAGCA AACTATGACT TCCCTAATAA 900
GGCGACGGCC AAAGCTGGCT CCCTGGCGGT CGAGCGCTAA TACAATTAAT CAGTCTGTTT 960
TCAGTTTTCT CACGACAGCA ATATTAACAG TTTGCTTTAT TCTGTTTATA TGGTGCTGAC 1020
AGGTCTTCGG CATGTTGCGC CTACTTGCTG GAGATTAATG GCCACTCTCA TATTGAGGTA 1080
AAAACCAGGC AGGAAGAGAA TGCCTTTTAC GACTAGATAA GAACTGGATT CTCTTGCTTT 1140
TTTTTGTTCC CCATCAACTC CTCCCTCTTT CAGTTTCTAT CAGGGATATA TGAGATTAGT 1200
TAAGTCCAGC AAGTTCACCT CACTGTTTAA ACTCCCCCAC TTTAGATGTC GTATCCTCAG 1260
GTAAAACAAA GGGAGCCTTA AATATTGATT TTGGATAAAC TCATTACATA TAAAGGTATT 1320
GGTGACTAAC TTTGTTTTTA AGAAGTCAGA TTCAGCCTGG GCAACATGGT GAAAGCCCGT 1380
CTCTACTAAA AATACAAAAA TTAGCCAGGT GTGGTGGCAT 1420
|
