| Tag | Content |
|---|
EnhancerAtlas ID | HS133-04954 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr10:112135410-112137260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr10:112137212-112137227 | TGGCCTTTGATCTCA | - | 6.28 | | ZNF263 | MA0528.1 | chr10:112136324-112136345 | GCCCCTTCTCTCCCTTCCTCC | - | 6.21 | | ZNF263 | MA0528.1 | chr10:112136343-112136364 | CCCTCTCTCCTCTGTTCCTCC | - | 6.21 | | ZNF263 | MA0528.1 | chr10:112136335-112136356 | CCCTTCCTCCCTCTCTCCTCT | - | 6.49 | | ZNF263 | MA0528.1 | chr10:112136063-112136084 | CCTCCACCCTTGCCCTCCTCC | - | 6.86 | | ZNF263 | MA0528.1 | chr10:112136327-112136348 | CCTTCTCTCCCTTCCTCCCTC | - | 7.31 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_38156 | chr10:112135153-112137228 | HUVEC | | SE_61384 | chr10:112100132-112156157 | HBL1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr10 | 112136840 | 112136884 | | chr10 | 112135607 | 112136796 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I110375 | chr10 | 112135499 | 112136986 |
|
Enhancer Sequence | AAGACACACA TGTGAGCGGA GTGTGTGTGA AATAAGAAGA AAGCCCAGTT GTAATAACAG 60
TAATTCTGAT CATAACAGCA GTGGCGCTGA CTGGGCACTC AGTGTGTTCT GGGCCTCGTG 120
CTCTACCTGT GGTTTCATTC TCACCCATGC CGCGATGAGG TAGGTACTGC TGGTGCCATC 180
ATTGGAAGAG AATGCTCTTT CATCCACTTG TTTCCTCCTT GCACCCCTTC ACTCATCACT 240
CCTTGAGCTC ACGCTGGGGG TTGTCTCCAA AAACTGGTCC AGATGCCCAG TGAGAGCAGC 300
CTGACCCTGG CCTGAGGCCT CCCCCAGCCA TGCTCTGGGT CTGTGGCTTC ATTTACCCAC 360
ATGCTGAGCA CCTCCCTCCT CCATCCATGC CCTCGCGGGA CCAGCTGTCC TCCCAGCCCT 420
GCAGGCCTTG AGCCTGTGCA TTGCTCAGCA AGCACAGCTG CTGGCGCCTA CCCATCCTGC 480
CCGGCCAGCT CACCGTGGGG CGGGCAGACA CCACAGCCTT CACCCAGCCA GGGCTTCCAC 540
ATCCCTCTGC TTCCCCATCC AGCACGCGCT CCTGACACCA TGCTCTGTTC GGGCTTTGTC 600
AGAGGTCCTG GCCCACGGCC TGGAGAGACC CCACGGCCCC AGCAACACCA CAGCCTCCAC 660
CCTTGCCCTC CTCCCCAGGG CTCGGCGTCC CAGTGTCCAT CCAGGAAGTC TGTCCTTCCT 720
CCCCAGGCGA CTTGGCCTTG GCCAGGGAGC ATCCTCAAGT GCAATTTCCG TCCAACTTTG 780
TCCCATGACC GCTGTGCCGT GGAAACGCCA CCCTCCACTC CCCTCCTGCC TCCGGCGCCA 840
CCTCAAGGCC ACTTCCTGTG TGACCTTCCT GCTCCTGGGA TCAGTCATTC CCACACTGGC 900
TGGTGCTGGG GCCAGCCCCT TCTCTCCCTT CCTCCCTCTC TCCTCTGTTC CTCCCACTCT 960
CCGGAAGGGA AGAAGGTCTG TCACCAGGCC CACAATTGAT TAATAGCCCA GCTTTCACTG 1020
ATAATTCCAC CTCTGGGGGC TGCAGCACAA AGGTTTGAGT AAACATAGTG ATTTTCTTTA 1080
AATACACATC CTCCCCACAA AGTAAAGTTT GTGACCCACC AAGGCCAGCT GACCCAGCAA 1140
CTGTTTTCAC CTCGGTGTCC TGGTTCTCTC CTCCGCCACC CCCCATGGCA AGGGTGTGGG 1200
AACAGCTTGG GATTCAGAAT CCCCTTGGGG CCCAGGGCCC TCACCCTACT TTGGTGAAGC 1260
CTTTCTAGAC CCTCTTCAGC CTGAGGAAGT TCCTCTCTGC TCCTCCCCTG CTGCCTCCTG 1320
GACCGTCCTT CAGGCTCAGA GCTCCTGGTC CCTGCCACTG CTGACCCCTT CAATGGTGCC 1380
TGCCACCCAC TCCAACAAGG AGCAGAGTAA CCAGGCCAGC CTGTTGCTCT TCCATTTTAA 1440
CCTGCCATTC CTGGCTGTCC CTCTTGGACT TGCGAGGTCA AACATTCCTG TTTCTGAGCT 1500
CCCGCCTCTT TCCCCAGCTT ATCTCCATAA TGTGTTTGGA CCCCCTCTCC TGCCTCTACT 1560
CTCATGGCCT CAGTTTTGAC CTCCTCTGCC CAGTTCCATG CCCTACTTCA GTTGCAGGGG 1620
CAGGGGATTA GAGGCCCTGG GGACTGCACA CGCTGCAGGA TTGAATGCCT CAGGGGCAGG 1680
AACTTGCGGA GGACAGAGTC CACTGCACGA GCTAGTAAAA AACTCCATCA TTGAGGGTCA 1740
CAAAACTGAA GGTCTTGATT CCGAGCTCTT CAGAGGGACC CTTGAGTGGG GCTCTGGTCC 1800
TGTGGCCTTT GATCTCATAC TCAGTCCATT GCAGCAGATG CTGTGGTCAC 1850
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