| Tag | Content |
|---|
EnhancerAtlas ID | HS133-21661 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:43111960-43114020 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT1 | MA0137.3 | chr22:43113939-43113950 | TTTCTAGGAAA | + | 6.14 | | TCF7L2 | MA0523.1 | chr22:43113457-43113471 | GAAGATCAAAGCCA | + | 6.24 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27285 | chr22:43112098-43114092 | Esophagus | | SE_42360 | chr22:43112008-43114137 | Lung | | SE_48740 | chr22:43112016-43114076 | Right_Atrium |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 43112173 | 43112912 | | chr22 | 43113109 | 43113947 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I042716 | chr22 | 43112118 | 43113806 |
|
Enhancer Sequence | CCTGAGTAGG TGGGATTACA GGAATGCACC AGCACACCCA GCTAATTTTG TATTTTTAGT 60
AGAGATAGGG TTTCTCCATG TTGGTCAGGC TGGTCTCGAA CTCCCGACCT CAGGTGATCC 120
GCCCGCTTCG GCCTCCCAAA GTGCTGGGAT TACAGGCATG AACCACTGCG CCCGGCCTCA 180
GAAATATAAT TTAAATCTTC AGATATGGAG CCCTAACCTG CTCTCTCCCA CTCCTACTCC 240
AGGCTCAGGG CACACTTGCC TCACCACAGG CTCTCCCAGG GCATAGGAGG GCGAGTGGGG 300
TGCATGACCA TCCTCTCCAC CACTGGGGTG AGTGGCAAAT GTGATCTCAC TGTTGTTTCT 360
GTTTGCACTG CTGACGGGGT GAGAAGGCTT CTCCAGTGTT GAGTTAACAT TTATTAAAAG 420
CTCACTGTCA GGCCTGGAGC TGTGTGGTTT AATAGTAACA ATGGCGTGTA TTTTCTGAGC 480
ACTGACCATG TGCAGCCGTT GGTCAAAGTG GTTTCCTGCT TTGACTTGTT CAATCCCTCA 540
CCATCCTGTG TGGCAGGTCC TCTTATGATT AACTACAGTG TAAGTGTAGA GGAAACCAAG 600
GCCTGCTGGG CAGCGGCAGA GCGGGGTTCA AACACCCTTT GCTGGGGGAA AGGGGTCTGT 660
CTACCTGTGG CCCAGCCTCA TTTGCCTGGG GCTGCACCAG GGCTAGGGGC TCAATCTCAC 720
TGTGGCCAAG AGGAGGTGCT TGACTCTGAG ACTCAGTCTC CTTGTCTGTA AAATGGGAAT 780
AACAGAGCAT GGTGGCTGAG AGGGTCTGGT AAGGTCAGGT AACAGTGTCT GGCTTAATGG 840
GTAGAGGCCT ACCCCCACCT GAAGGGGAAG GAGCAAATGA TGGTCACAGA TGATCAGGGC 900
TCTCTGGGTC CCGTAACTAT ATCTGGGACA ATGACTTTCA AACAGGTGAA GACAGACACT 960
CTTCCTGTTT CGCTCTCATG TGCTGGTCCA CCTGGCTCCC TGTCTGCCAG CTGACTGCAC 1020
AGCGTGACCG CAGAAGGCTG TGGTGCTCCT GCTGGAGTAG GCTTGTGGTG GGTGACAGTG 1080
CGGGCACAGG GGAAGGTGTG TGGGCACAGG GGAGGGTATG TGGACACTGG TCTGGAAGGG 1140
AAGGGGGCTC CCCTAGTCCT GTGGCCAACT GCACAGCTGG AAGCTCCTGA ACCCCCAGGA 1200
TATGTCCAGA GGGAAGACAA AGGTGGCAGA TGGGAGAGGA AAAGGCACTT ATTCAAAGAG 1260
CTGCCACTTC CTGATAGCTA CAAGAAACAG AGCCTCGGAG AGAAGAGCAA TTCCCAAGGG 1320
CTTGTGGTTG GTATGTGGAC AGCCTGCTTT GAACCTGGCC CTGCATGGAC TCACCCTGAA 1380
CTAGGCTCTC TCCTCCCTGC GTAGTCATCA ATGGGAGTGT TCACACCTGC TCCCTCCCAG 1440
GGAGGAAGCA CCAAAGACTG GGGCCCTCCC CTCCGCTGAC TTCCAACTCC CTCTGGGGAA 1500
GATCAAAGCC AATTCATCAA GTGTCCCCCA AGCCCCTCCC TCTTGCCTCC TGTCCTCACC 1560
AGCCCGGGAG GATCCTTGGG AGCAGCACTG CATCCTCCCA CCTCCTCAGT CCTCGGAGAC 1620
CTCAGCCTAT CAACCTGTCC CTCCTTCTCC TGGGCCTGAG GGAGCTGAGC TCTCTCTTCT 1680
AGCTTTCCCA TCAGCTCATA AATGCAGCCA AGTCTCCCTC ATCAGAAAGC ACACACACAG 1740
ATAAAGTAAA ACAAAAAACT TGCTGCTCCT CTCTATCTCT CTGTCTCACA GACATACACC 1800
CACACACACA CCCACGCACG CACAAACACA CCCACAAATA AGAGCCAAAT GATAAACTGG 1860
GGAAAGATCC TTGGCACACA AAGACCAGAC AAGGGGTAAA ACCTTACTGA TGAGCTCAAA 1920
CCAATCAATA AGCAACACAC AAAGAACCTG GCTTCTCGTA CTCTGACCCA GGAGTTTCAT 1980
TTCTAGGAAA TACGAAGAAA TATCTAGCTG GGTCCAGATA CAGCCATTCT AGAAGTTCAT 2040
ACGCACTGAT TACCAGGTTA 2060
|
