| Tag | Content |
|---|
EnhancerAtlas ID | HS040-09797 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr13:99860640-99861960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr13:99861253-99861265 | TGCCTGGGGGCA | + | 6.04 | | ZNF263 | MA0528.1 | chr13:99860989-99861010 | GGAGGAGGAAGGAGAGGTGAG | + | 8.12 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27322 | chr13:99860428-99862098 | Esophagus | | SE_59717 | chr13:99855449-99919046 | Ly4 | | SE_62615 | chr13:99851542-99891972 | Tonsil |
|
| | 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 |
| GH13I099208 | chr13 | 99860429 | 99862098 |
|
Enhancer Sequence | TTAACTGATT CAGCAGATAC TTACTGAGCA CTCCTGTGGG CCAGCCGGTC TCCTAGGTTC 60
TCAGGATTCA ATAGGAAGTA AAAGGCCACA TAAGGTGATG ATCTTAGGTG ATAGAAGTCT 120
TGAAATGTAG GCTCCATTTA AAAATTAAAA GTGTCCAGTT CAATATATTA ACACTTCAGT 180
CTTCATTCAA AGATTAGACT TTCCCCCCTT TTTTTCCCAG TTAAGACTTG TAGTTGGCAA 240
CCATCTCTGT CCGAAAAAGC GGTGTGACAG GCTTCTGGTG CGTTCGGCTC CTCTCTGTCC 300
CTCAGATTTC TTGTGTCTGA CTTCACTAGT TTCTGGATTG AGTGGAATAG GAGGAGGAAG 360
GAGAGGTGAG GCTCTCAGAT TGTTCTTCTG TGGCTCCCTG AGCCTCGCAC GTAGTTAAAG 420
CTGACCCTGT GTCCTGCAGG TGCTTCAGTG GGCTCTTCAG AGACTCCCGA CTTCTATCCC 480
TTTTGCCTCC TTGACCTGGG GGTTTGCATC TTTATTTTGG TCGATTTATT TTGGCCAGTT 540
TATTTTGGTG ACTCCTCAGC ACCTAGGAAC TTAGATCCCC CTATAGTTTC CTCCTGCTGG 600
AGTCCTTTTG GCCTGCCTGG GGGCACTGTT GTTTGAACCT AAGACCCTCT GCTGGCTCTC 660
GCGCACAGCC TGGCTGGGAC TGCGTGTTCC TTGCCCTGGC TGTGCATGTG GGTCCCAGTG 720
CTCAGCACGG CTTTTCCAGC TCTCTAGATT TCCCAGGTTG GAGATCCACT GTACCCTTGC 780
TGGTCACAGA TTTAGCACAT GAAATAGGCC ATCGAGCCCC TACCTCAGCT TGGTATGAAG 840
GTGTGGCTGT ACTCACAGCC CCTCAAGGAT TCACTTCACA AAGCCCCCTC CTCCTGTCCT 900
GTCTTCACGG GAGGGAACCC TCACATTCCA CTGTCTGTAG CCCTGACCTG GCTGAGAGGA 960
CTGTGGGAAT CAGGGGACTG CCTTGCAATC ACTCTTGGAA AGTTCTGCAT TCTGCTATGG 1020
AGCCTCCCTT TGGTGGCAGC AGCCCTTCTC TTTTGGTACC TTAGTGGAAA TTCCTGTTTG 1080
ATCATCTTGT TTTGGTTGGT TTTCTGTTTG TGGGCCAGGA ACTGTTTGGC TCTCTTCTTT 1140
AAGGCAGGCT TTAGTGTTTA TACTTTTCTG CTGTAACCAG GCCTGGGTTG CCCAAACCTG 1200
AACAGCTCGT TTACTCTTGG GGACACACTC TTCCCCACCA GTCTTAAGTT TTTGGGGGCT 1260
GTATTATTGA AACTTCCAAG GAATATACTC TTCATAAATT TTAGCGGCTG GGCATAGTGG 1320
|
