| Tag | Content |
|---|
EnhancerAtlas ID | HS040-14574 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr17:4150640-4152100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr17:4151109-4151120 | GGTGACTCATT | + | 6.02 | | Klf1 | MA0493.1 | chr17:4151503-4151514 | GGCCACACCCA | + | 6.62 | | ZNF263 | MA0528.1 | chr17:4152061-4152082 | AAAGGAGAGGAGAGAGGAGAG | + | 6.15 | | ZNF263 | MA0528.1 | chr17:4152066-4152087 | AGAGGAGAGAGGAGAGGAGAG | + | 6.99 |
|
| | 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 |
| GH17I004246 | chr17 | 4149624 | 4152890 |
|
Enhancer Sequence | GTAGCAGCTG CCTGGACAAT GACACAAGAT ATAAACTACC AAGGTAATGA GCAGAGAAGA 60
AGCTAGATAA AAGGAGGGCT TTAGCATGAT TTGGGGCTCT TAGTCACAAA ATTACAGATG 120
CTCCCCCACC CGGCAGCTTT TGTCGGGGGA AACCCAAAGG ATCACTAATG CACTCAGGCA 180
GCTTATGAGC ACTTACCAGC GCTACTTCAA TTGCCATACC ATTTCACAGT ATAATGGAGG 240
AGTGCTTATG GCTGAGACAT TACCAGCCCG TGGGGAATAC TGTCTGCTTA CAAACAGCAA 300
TGCAAATGTG TCCTTGAAGT GTCACCAAGC TGTACAGTTC TTACAAGAAA AAGTACAACA 360
TTATTCTGAG CAAAATGGAG AGAGAATTTA CAGTGTGCAG GTTCTAGGGC CAGACTGACT 420
GGGATCAAGC CCAGCCCCAC TACTGCCTAG TTTTGATACA CCTTAGGCAG GTGACTCATT 480
CTCTTCACCT GCAAGGATGT TGTAAACACT GAAAGTACTA ATACATGTAA TAACCTTAGA 540
ATACAACCTG CTCTGCAGTA GGTGGTCAAA ATATATTAGC TATTATTACA ATTCTTAGAA 600
AGGCAACCCG GGGTAGTCAG TCCTGTGTTG CAAGATTCTC CCTGCACACT GATAGCCCAG 660
AGCTCGCATT CCAGAGTCTC ACTGACTGGG TTTGACCCCA GCTTACCCAT TTACTAGCTG 720
TGTGACCTTG GGCAAGTTAC TTACTTCCTC TCTGTGCTTC AGTCTTCTCA CATGGAAAAT 780
GAGACTAATG ATACTATCTT AGAGCAGGTG TCCCCGACCT CCAGGCCGTG GACGGGTACT 840
AGTTTGTGGC ATGTTAGGAA CTGGGCCACA CCCAGCAGGA GGTGAGCTGC GGGCGAGTCA 900
GCATGACCAC CTGAGCTCCG CCTCCTGTGA GATCAGCAGC AGCATTAGAT TCTCACAGGA 960
GCGTGAACCC TCCTGTGAAC CGCGCATGCG AGGGATCTAG GTTGCATGCT CCTTATGAGA 1020
CTCCAGTGCC TGATGATCTG AGGTGGAACA GTTTCATCCT GAAACTACTC CCTTCCCTAC 1080
CCCATCTATG GACAAACTGT CTTCCACGAA ACCAGTCTCT GGTGCCAAAA AGATTGGGGA 1140
CCACTGTCAG AGAAGTACGT GTAAAGTCAT TAGGATAGGT TAAATCACTC GGAACAGTGT 1200
CTGGTTTAGT AAGGCTTACC GCTGCTGCTA CTCCTCTGCC TACTTATTCT TCATCAAGTG 1260
ACCAGTTTTC AGCCGTGGTT TTTTCTTTGT CCCCTTCCAA CTTTCATTTG AAAAGCAAGC 1320
CTAGAAATTT AATTAGCCGG GCATGGTGGC GCATGCCTGT AGTCCCAGAG ATGATGCCAC 1380
TGCATTCCAG CCTGGGTGAC AGAGCAAGAC TCTGTCTCAA AAAAGGAGAG GAGAGAGGAG 1440
AGGAGAGCAA ACCTAGAAAT 1460
|
