| Tag | Content |
|---|
EnhancerAtlas ID | HS133-29303 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:101707120-101708630 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr7:101707142-101707159 | AGTTTTCCAGGAATTCA | + | 6.16 | | EWSR1-FLI1 | MA0149.1 | chr7:101707901-101707919 | CCTTCCTCCCTCCCTCCC | - | 7.28 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_34891 | chr7:101704768-101709954 | HeLa |
|
| | 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 |
| GH07I102061 | chr7 | 101704436 | 101710091 |
|
Enhancer Sequence | AAAACAGTTG ATGCTACAGC TTAGTTTTCC AGGAATTCAG TATCCCTGAG TCAGGCAGCC 60
TTATCTGTCA TCCTAGAACT CCAGGACAGC CCCAGGTGGT GGTGGGAGGG GCCGCGGCTG 120
GGAGATGGAG CTGCTCTGAG CCTGCAGATC AGGGTAGCAT TCCTGGGAGG CGCCTTCCAG 180
GCGGAGGGGA AATTGCTCAT GTGTTCTGGG AACTGGGAGT GACTGGGTGT GGCAGGAGTG 240
TGAGGCATGG CAGGAGGTGA GCCTGAAAAA GAGGCTGATC CCTCAGAGCA GGACAGGTTT 300
TACCCAAGGC TGCAGGCCAG TGTCTAACCG TCTCTAGATC CGTCCTGGTT TAGCTTCTTC 360
CAAATAGTTT TGTGTCTGTG TGAGAGTGTG TGTGAAACGG AGTTTTGCTG TGTTGCCCAG 420
GTTGGTCTTG AACTCCTGGG CTCAAGCGAC TCTCCCACCT TGGCCTCCCA AAGTGCTGGG 480
ATTACAGGCA TGAGCAACGG TGCCGGCTCT AAATGGTTTT AAGGGCACGG TACCTACCTC 540
AAGCTAACGT GCAGGCAGGC ACGAGGTAGC TGGAATTCTA GCCTAGGATT CTCTCTTCAG 600
CAATTCTTGC CTTAAGACCT CACCTTAGAC GTTTGCTCAT TCACAGATCC CTCCCCTTCT 660
CAGAGGGAGC TGTGTTACCA AGCCTTGGCT TGTACCTCCA AGGCATGCAG TGGATGGGCT 720
GAGCTCCCTG CAGGGAGTCA GGCGGGTGTG TGGGGGGCAT GAAGGTGAGC AGGACACTGT 780
CCCTTCCTCC CTCCCTCCCA CGGATGCTCT TCCTGGCTGG TAGCCATGTG GACACCTGGG 840
GGGAAGCTGT TCTGTGTGGC AGAGTCACTG TGTTGTGTCT GGTACTGGGG CCCTTGCCAG 900
GGTAGGTCAG TGACTCGTCC AGGCCCTGGA GGCTGCTGCT GTCCCCTCCT CGTGCAGAGG 960
AGGTGGGGCT GGCAGTCAAA GCCCAGGCTC CCTCCCTCCC TCTAGACTCA GAACAGCCCA 1020
GGAACCCAGC TCGAGGTCTG GAGGAAGTGA TGTGTGCATT GGGTCTTGCA GCATAGATAG 1080
GTTTTGAGTG GACGGAGAGG TTAGCGAAGG GTGTTCCAAG TAAGCAAAGC ACGGAACTAG 1140
GAAGTCACTG GCTGCAGCAG GGAAGTCACA CAAAGGGACA ACCTACCACA GACTGGGTGA 1200
GCTGCAGAGG GAGGATGGAC TAAACTCCAA CTTCAGGGTC ATTCTGGTTG TTTTTTTTTA 1260
AGACAGGGTC TCACTTGGTC ATCCAGGCTG GAGTGCAGTG GCTCAATCAT AGCTCACTCC 1320
AGCCTTGAAC CCCTGGGCCC AAGCGATCCT CCCACCTCAG CCTCCGAGGA GCTGGGACTA 1380
CAGGCGTGTA CCACCGTGCC TGTCTAATTT GTATTTTTTT GTAGAGATAG GGTCTCACTA 1440
TGCTGCCCAA GCTGGTCTTG AATTCCTAGG CTCAAGCCCT CCTCCCACCT CAGTTTCCCA 1500
AAGTGCTGGG 1510
|
