| Tag | Content |
|---|
EnhancerAtlas ID | HS147-00843 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:27492390-27493630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:27493605-27493623 | CCACCCTGGCTTCCTTCC | - | 6.17 | | EWSR1-FLI1 | MA0149.1 | chr1:27493563-27493581 | CTCTCCTTTATTCCTTCC | - | 6.25 | | JUN | MA0488.1 | chr1:27492999-27493012 | ATGACCTCATCTA | - | 6.15 | | JUND(var.2) | MA0492.1 | chr1:27492998-27493013 | GATGACCTCATCTAT | - | 6.7 | | ZNF263 | MA0528.1 | chr1:27492898-27492919 | TCCTTCTCTCCTTTTTCCCCC | - | 6.15 |
|
| | 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 |
| GH01I027166 | chr1 | 27492577 | 27494074 |
|
Enhancer Sequence | TGGAAAGCCA GGATGGGCGG ATCACCTGAA GTCAGGAGCT CGAGACCAGC CTGGCCAACA 60
TAGTGAAACC CCGTCTCTAC TAAAAATACA AAAATTAGCT GGATGTGGTG GCAGGCACCT 120
GTAATCCCAG CTACTCTGGA GGCTGAGGCA TGAGAATCGC TTGAATCCAG GAGGCGGAGA 180
TTGCAGTGAA CCAAGATCGT GCCACTGCAC TCCAGCCTGG GTGACAGAGT GAGACTCTGT 240
CTCAATAAAT AAATAAATAC ATAAATATAT AAATACATAA ATAAATAGCT GCCCTTGTCA 300
ATGTTGCCAG TGACCCTCCA TGTTGTTCTA TCATATGGTC ATTTCTCGAT CCTCATCTTT 360
CTTTCCCCAT CAGCAGACTT CAACATATAT AATCACTTGC TCCTTCTGAG AACACTTTCT 420
TCAAATAGCT TATGAGACCC CGCAACCTTC TGGCTTTCCT CCCACTTCAT TGGCTGTTCC 480
TTCTCAATTT CCCTTTGTTG ATTCCTCCTC CTTCTCTCCT TTTTCCCCCT CTGCCACAAC 540
CTCTAAATAC TGAGGGCCCC AGGGCTTGGT TCTTGCCTTT TCACTGCTCT GTCTACATTC 600
TTTTCTCTGA TGACCTCATC TATTCTCATG ATTTCAAGCC CCATCTATAT GAGGACAACT 660
CATAGATTTC TATCTCTAGC CCAGTTCCCT ACTGTAAACT CCAGACTCCT GCATCCAACT 720
GAACATTCAA CATTTTTACC TGGTCGTGCA ACAGGCATCT CAAAATCAGC ATGTCCAAAA 780
CTGAACTCCA GACCTTTCCA ACCCCTCCCC AAACCTGCTT CTCCCACTGT CTTCCCCATC 840
CAAGAGATAG CCTCTCCATC TTCCCACTTA CTCTGGCCAA AAACTTGAGT CATCCTTGGC 900
TCCTTTCTGT CATATCAATC CTCCACAAAT AGTGTCAATT CAATCTTCAA AATATTTCCA 960
GAATCCATCC ATTTCTGACC ACCTCCATTG CCCACTCTGG TCCAAGCAGT GCCATTTTCC 1020
CCACCCAGAT TATTGTTTCA ACAAAGCAGC CAGAAGGATC CCTTTAAAAG CCTAAGTCAG 1080
ATGGTGTCAT CCCCTGCCAG ACCCCCACCT CGGGGTCCTT ATTATGACCT ACGAAGCCCC 1140
ACCCAGTCTA CTCCCACCTC TCTCTCTGGC CTCCTCTCCT TTATTCCTTC CTCTTCCCTT 1200
TTCTCTCCAC GTTAACCACC CTGGCTTCCT TCCTATTTAT 1240
|
