| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02058 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:110671940-110674180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr1:110671970-110671980 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr1:110671970-110671980 | GGCACGTGCC | - | 6.02 | | RREB1 | MA0073.1 | chr1:110674010-110674030 | CCCCCAACCACCACCTGCAG | + | 6.41 | | ZNF263 | MA0528.1 | chr1:110673128-110673149 | AGAGCAGGAGCAGCAGGGGGA | + | 6.13 | | ZNF263 | MA0528.1 | chr1:110672990-110673011 | GGATGAGGGAGGAGGGGAGGT | + | 6.66 | | Zfx | MA0146.2 | chr1:110672069-110672083 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 110672728 | 110673048 | | chr1 | 110672711 | 110672989 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I110130 | chr1 | 110672728 | 110673048 |
|
Enhancer Sequence | CCCTCAGCCT CCGGAGTAGC TGAGATTATA GGCACGTGCC ACCACACCCG GCTAATTTTT 60
GTATTTTAGT AGAGACGGGG TTTCCATGTT GGCCAGGCTG GTCTGTAGCT CCTGGCCTCA 120
AGTAATCCTC CCGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGTGTGAG CCACCACGCC 180
CAGCCTAAAT TCTTTTGACT TTGTTGCTGC AGGGGAGTGA AAACTTAACC TTGGTAATTT 240
TGGGTGGGGA CATTTGCCTT TGCCATTGTC TGGTCCTGAA GGTCTGTTCC GGTTGTCTCG 300
GAAAGCCCTA ATCCGTGACT AGCCCTTGCA GCCTGTGGCT CCTCTGCTCC TTTGACCCCA 360
GTCTGAGGGG GATGCTGGGG CATCTGAGAG CAAGCCGGAG GGAAGTCTGG TCTCTGAGAA 420
CCACATGCTG CAGAGGATTC AGGGGCCCTC TGTGACATCC ACCACCCGTG ACTCTTTGGG 480
CCTTTGGGGT ATGGTTTGGG AAATCCTGTC CCCAGCACAC TGTGTCCTAG CCAGATGCTC 540
TGGGCAGGGG TGGGAGTGGG GAAGGGAGCA CCGGACCAGC TGTGAGAAAT TTCCCCACGT 600
CCCCTCTTGG AGTCCCTTCC TTCTCTAGGT GCTGGCCACT CTCAGGAGTG TGTGCATGGT 660
GGGAGCATAT GGGGAAGGTG GCGGGGGGCG GTGTTTGCAG ATGTTCTGGC CAAGGGAGCC 720
TCTGAATGGG GCATTGGGGA CCCCGAGACC TCTCAGCAGG CATTCTAGAG GCTCGTCGGC 780
TGCCCTGCTG TTTGGATACT CTACAGAGCC GGGATTTATG TCCCTTCCCG GCTCCCACGC 840
CTCTTGCTGG GGAGGGTGGC TCATTTTTCA CGGGTGCCGC GTGACTTTCC AGACTGTATT 900
TTCAGCCTCG GTTTGACGTC AGGCTCTCAC GGTCCCAAAG GATGGGCTTT GTACATTTCC 960
AGGCCGCAGA CCGGAGCCTC CCATCCCTTT GGGCCTCTTG GGCGGTCCCT ACGGCCACCT 1020
CCCGCAGCTC CCTGGGGGCG GGGGACCGCT GGATGAGGGA GGAGGGGAGG TACTGGGGGG 1080
AAAGGGCGGT TGGCGGGAAG GAAGTCCAGG TGAGACAGGC CCGCGTTGGG ACTATCGTGC 1140
GCGGTATGTC GGCCGGCAGG TGGGGCTGGT CCGGGCGCAG GAGGCGGTAG AGCAGGAGCA 1200
GCAGGGGGAG CCAGGCTGGC CGAGCTGGGG GGTGAGCACG TTTGTCTCAG GCAGCTCATC 1260
GCCTGACACC CCCGGGAACG GGCTCTGCCC CAAGGCCTAA AATGAGGGAA GATGAGGAAA 1320
TGGGGGTGGG GACGATGGAG AGGATGGAAG GGGCGGCGGG GGGGTGCGGT GGTCTGCGCG 1380
GTACAGCAGC GTCCCTGCGG GTTCCCCTCA TTTAGTCCTC AAAACAACCT TGCCGCGGGT 1440
TGTGGTTGTC TCTTTTCACA GACGGAGAAA AATTGTTGCG GGGAGACTGC TCTTGGCCTC 1500
CCCTCAGCTT TTGTTCAGCA TTGAAGGGGC AACATCTGTT CTCAGAGTTG GGCGCCCAGG 1560
TGTGCCTGAA TTTCATCACA GCCGCCCCAA AGTGCTGACC ATGGCTGTGT CTGGGTGTCT 1620
CCATCCTCAT CCCGTCTGTG AACTAGGGCT CCACCTGGGT CAGGTACCCC AAATACTGTC 1680
AGGAGACTTC AGTTCCAGTT TCTGCCCTAA CACTTTCTGT GCGACTCCAG GACAGTCATT 1740
TAACTCTCTG GGCCTCAACG GCCCCATTGC TTTGTGCTTA ATTAGGTAAA CATGTCCTGG 1800
GCTGAGGAAA TTTTCTCTGC AGCCTAGGCC CCATGCTGCT CCTCATCCCA CACCTGCTCT 1860
CTGGTTAATG TCATCCTTGG CCCTTGGCAG TCCCCGAGAA GGACCGCTGG AGTGGTCCTT 1920
CAGCCCTCCC TTGCCCTTAC CCAATCCAGG CAGCTGCCAG GTGCTGCTGC GTGTGCCCCT 1980
TAAATACCCT GCATTCAGGG TCCTGAATGC TGCCCTCAGC TCTGGCACTC ACGGCAGCCA 2040
TCTGACTGGC CTCTCGCTTC ACCCCCCTGC CCCCCAACCA CCACCTGCAG CTCATCCTCT 2100
GGCTTAAAAA AATCTCCTAT TCACTCATGG AGTAAATTCA TTACCTACCT CAGCAGGCAG 2160
TGGAGGGGGT TAGGCGGGAT GATGGACAGA AAGTACTGCA CACCAGGCCT GGTGTTTGGT 2220
AGATGCCTTT CTTCAAGGCT 2240
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