| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00288 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:9941660-9943760 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chr1:9943345-9943356 | GGGCAGGTGGG | - | 6.14 | | ZNF263 | MA0528.1 | chr1:9943724-9943745 | CCTCCCTCCTCATGGTCCTCC | - | 6.37 | | ZNF263 | MA0528.1 | chr1:9942711-9942732 | GAAGCAGGAGAGGAGGGGGAG | + | 6.69 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_26899 | chr1:9941501-9943467 | Esophagus | | SE_32383 | chr1:9941664-9942858 | Gastric | | SE_40969 | chr1:9942237-9945655 | Left_Ventricle | | SE_42671 | chr1:9941907-9945516 | Lung | | SE_49264 | chr1:9941997-9945462 | Right_Atrium |
|
| | 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 |
| GH01I009881 | chr1 | 9941604 | 9943264 |
|
Enhancer Sequence | TGCTGGGATT ATAGGCATGA GCCACCACGC TGGGCCCCAG CCTTGAAATT TTTAATAATT 60
TCTGAACAAG GGGGCTTGCA CTGAGCCCTG CAAATGATAC AGCTGGTCTA GAATGAGAAA 120
AAGAAGGTCA AGATGCTTCT CAAACTGCCA AGGGTTCCAC AACCTTAAGT AGACACTAAA 180
TGGACTCAAG AAGGATTTAC TGAAACTTTT CTAGGTACAC ACAGCCCTGA ACCAGGCTTG 240
GGGAGCACAA GGTACAGAAC TGGGGCCGTG ACACTGAGCC TGCATTCCAG TTGACTGAGT 300
GGCTGAGGAA ACCACACAAC ACAAGGCAAA GAGAAAACCA CACAAATAAT ACATGATAAT 360
GAGCCAAAAA GATATGTTAG GTCAAGACAC AAACCCTCCT ACAGTGCCAA CCACATATTA 420
TGTACTGTGC CAAGCATCTC CCCTGAGGAA AGAAGACCCA GGGCCTTAAG CCAGCATAGG 480
AAGTGGCAGA GCAAAGGGGT GTAGTGAGCT CTGCAGGAAG GCAGGGGAGA GGCTGGCTGC 540
CAATGGCTCC AGGGAGAAGT CACTGGAGCT GGGCCTTGAA GGATGAACAG GAGTTTGCTG 600
GTAGAGAGAA AGGGGAAGGC ACAAGACACA GAAGTTCAGC GAACAATTAC TGAGCATCTA 660
TTCTACGGCA GGCATTGAGA ATACACAGGT GAGCAAAAGA GCCACGGCTC ACATGTGATG 720
AGAGGCTTCC AATGAGCAGG GGGAGACAGA CACCAGTCAA GTCACCCAGA TCAATGATCT 780
CAGACACTGA GACAAAGAAC ATGAAGGTTA AGTTTGAGTC GCCTCGGGGA TGTGCGGCTG 840
GGAGCCTGGA GGAGAAGGAG GAGTTGGTAG GGGTGGCATA CACGTAGGAA GGCCCGAAGC 900
AGGAAGAGTT GTGGCTTAGG CCAAGTTAGA GCTGGACCAC AGGGGCACTC AGTGGGAGGG 960
GAAGAGGTGT TTCAGCAGAA GGAAGTCAAG CCTCAGCTTG AAAAGACCAC TGTGGCCAAG 1020
GTGTGGAGCA GAGGCTGGGG TGGAGCAGCA GGAAGCAGGA GAGGAGGGGG AGCAGCCAGG 1080
CAGGGGCTTG GTTGGGTAGA GAAGAGCCAG GAGGAGTGTA AGAGTGGGGC TGTGGCTGTG 1140
GCTGTGGGGA GAGGCCTGGC ACATGTCCAG GGTGAGGCCC CAAAGGACAG GCTGGACAGC 1200
TGGGACTGAG AAGCCCATGG AGGCGCAAAA GCAGAGGAAT GGCACAAGTG CACGTGCCCT 1260
TGGGATCAAG TCAGCACTAC GGTGAACATT TGCAGAGGGT TCCAGGGCCA GAATCGAAAC 1320
ACGGTGACAA GCTAGTTCCG GGAAACATCA GGGGCACTTC TGGGGGCTAC TTGGCCTGGA 1380
GTGAGAATGG GGGGCCTCAG GAAGAAAACA CGTGCAAGCA CGGGTGGGGC AGCCGCAGGG 1440
CAGGGGGCTC CTTCTGTGGG CACGCAGAGC CAGAGCAGTC AGGAACAGCG GGTGCCTGGG 1500
TGGCAGCAGC GGGACGGCGC AGGAGGGTAG GTCAGGGACC GGGGGAGCCT CTCTCTGGAA 1560
GGAAGTCCAA CCTGCCAAGC GGAGGGCATT GGGCCCTGGT CAGGAGATGA CTCGGGCAGA 1620
GTGGTCTCCC AGGAAGACCG GAGTCTGGGT GGATTCATGT GAAGCCCTGT GTGAGATGTG 1680
TGGAAGGGCA GGTGGGACAC CACAGGCAGG ACCTCACGAG GCCCAGGTGC AGGGCAGAGA 1740
GGGAGCAAGA ACAGTGAGAG CTGCTCCCGA GAGGCAGGAA CCAGTGGGTT TTCTATGAAG 1800
GAGGCAGAGC AGGGCAGGGG AGAGGTCCAC CTGCCCCATC CCATGTCTAC TCAGGCCCCA 1860
CAGGCTCCTG TCCCCATCAC AGCCCTCACT AAGCATGGGA CTGCCCCCCA TGCACATGCT 1920
CCAACAGGAC AGGGGCTGCT TCAGTAGCTG TAACAACCCC ATGCCAGCCT GATCCAGCAC 1980
CTGGTGTGTG GCATGGCAGG CCCACAAGGA GAGCAGGGAG GATGAGTGGC TTCTGCTCTT 2040
CTTCCTCTGC CTAGAAACCC TTTCCCTCCC TCCTCATGGT CCTCCTGGAA CTCAGTACTC 2100
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