| Tag | Content |
|---|
EnhancerAtlas ID | HS180-25527 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr2:27318210-27319590 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr2:27319378-27319389 | TAATTTAATCA | + | 6.62 | | ZNF143 | MA0088.2 | chr2:27319299-27319315 | CAGTGCATTCTGGGAG | - | 6.99 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35436 | chr2:27314252-27320244 | 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 |
| GH02I027090 | chr2 | 27313498 | 27320068 |
|
Enhancer Sequence | TTCCAAAGTC AGCCCCAGAG TTGCCAGCCT GCAGCATGGC ACCAAGGAGC TGGGGTTTGG 60
GTGTGTAAAA GAGATCAGCC CCCCAAAGTT TCCAGCATGA TGAAGCCAGG CCACACACCA 120
TTCACAGCCA TTGCTGAAGG AGGGGAAAGG AAACATGGGG TCAGCAGATC AGGGTCATCT 180
AACATGGTGC TGACCTGGGG GAAGGGGCTA TCCCTCCCTT CAGGGTCCCA GGCCACTCAA 240
GAGAGGCCCC ATGGGCCTAG ACACTTCTTA TCCCTTGCAG ACTCCCTCCT GCAGGATTTT 300
AGAGGTTTAG TGTACTAAGA ACCTAGTACG TGCCAGGTAC TGTTATGGCT GAGAGGGCCC 360
AAGCCCAGCA GCCCTCAGGT TCAGGCTGTT CCTACGGCCC AGCCTGACTG CCGGACCTGG 420
AGGAGGGGCA GCCATCCCTG GGCTTCATAT GTGCAGTGAG TGTGAGTAGG CAGGCATATG 480
TGCTACAGGT GACCTTCGCA TTGGGCAATC CTAGTCAAAT GCTTGTTAAG CAACAATCCG 540
TAGTAACCCT GATCAAGGAC ACAACATAGC TATTTACAGG AGAGGAGCTC TGAGGAGAAA 600
TGTTTCTTGC CCACTGGCCT CAGTCCAGGC ACATTCACAC ACATTACCTG CAACTGCAGC 660
AGGCTGCAAG GGGGCTGGGG GTTTCAGCCC CATTTATCAA TGTGGAAGTT GCCTCCCAAA 720
GGCCCGGGCA GATCACACAG CTATAGTTAA GTGGAAGGAC TCGGCTACAG AACGTGGAGC 780
GGGGACTTTG GCTGAGTTGA GGTCTCTGGC TCAGGAGGGT CAAGGCAGAC CTCTATCGGG 840
AGTCCCCTTT CCTAAACCGG CCAAACACAA ACTCTTCCTC AAGTGCTACC TTGACCTCAG 900
GGTTGCAACG GGGAGCTATT AAACGCAGGA CAGGGGTGCC ATAGGTAAAC CCCAACGCTG 960
GGGCGCCAGA AGTGAGGGGG ACCAGACAGC CCAGGCAGGG GGTCGCGGGC TTTATACTTT 1020
CCCAGGGCTC TGCCTGTGGG AGCCGTGTGC TGCTGCAAGG GATTCTGGGA AGTGTAGGCT 1080
TGGCGCTCTC AGTGCATTCT GGGAGATGCA GTCTCCAAGG CACACAGACC TTGCCAGTTG 1140
ACATGTGTTG CAGTTCAGTT TACCGAGATA ATTTAATCAC AACCTCAAAC TCAGGAAAGG 1200
GCACCCCAGC AGACTGTAAC AGGGACAACC CTGGAGCTGA GCCTGAGAAT CCTGTGCTGT 1260
GGATCCAGCT TCCTGTCATG CTGCCAGCAG TGCAGGCACA GGGTCCACAG CTGCCAGTTA 1320
GAGATCCTGG CTCTGCCTGA CCCCATCATG CTCCTTCTTC TCTGTCTTTT CCATCCTGTG 1380
|
