| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00268 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:9760210-9761500 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr1:9761256-9761267 | CCACACCCTCC | + | 6.32 | | ZNF263 | MA0528.1 | chr1:9761050-9761071 | GCCCCCTACTCCCCTTCCTCC | - | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_11127 | chr1:9760165-9765942 | CD20 | | SE_17476 | chr1:9760347-9761859 | CD4p_CD25-_CD45RAp_Naive |
|
| | 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 |
| GH01I009698 | chr1 | 9758747 | 9761309 |
|
Enhancer Sequence | GACAGAGTCT CACTCTTGCC CAGGCTGGAA TGCAGTGGTG TGATCTCGGC TCATTGCAGC 60
CTCCCCCTCG CAGGTTCAAG TGATTCTCGT GGCTCAGCCT CCCAATAGCT GAGGTCAGAT 120
CCCTCAGACG TTCACAGCTG GGACGCCGTT CTTCCACCTT GGGCTCCAGA AAGAGCACCA 180
AGGAGAACAT TTCAGGACAG ACTGTAAGGG TGGCGTGGTG TCCTGGCCAG AACCCCATGT 240
GCGGGAGGGC TCCGCTTTGC ACAGCTGTTT CTGTGGATCA TGCTGGCCAG GAGGTGGGAA 300
GGTGAAAGGA ATTGTGTTCT TATCCTGTTT CCTTGGATAT TTTATGAGTG ACTTAGATGT 360
GGACACAACT CATGCCTCAG GATTCTGGAT GAGTAAGTGA GGAGGGATTG GTCACCGTCC 420
ATCACTGGGT GACGCGACCC CAGCTCCCCG CTCTGTGTCT AGGCCGTCTC ACCTGCCCCT 480
CCCCGGCTCC ACATCTGTCT GTAGCCTGCT GACTCCACAG ATCTGTCCCC CGCCCTCCCA 540
CCTGGGGAGT TTGCCCCTGG CGGTCTTTAC GTGGCTATTC ATTAAGCAGC TGAGATTCAT 600
TTGGTCTAAA ATGGGGCTCC GGCTGTCTTA TCCCACCAGA AATCTCTTCC TTTCCTGTCT 660
CAGTAAATTC CCACCACCAC TCCCATCTCC CAAGCCCAAA CCTGGCTGTC ATCCTCACTT 720
CCTCCTGCAC CGTCCCCCAA GGGTCCCTCT GATTTAAGTA TGTCTGGATT CCGTTGCTCT 780
CCAGTGCTGT CTCCTTCTGG GTCAAGCCAC TGTCATTAGT GGCACCGGCC TCCTTCCCCT 840
GCCCCCTACT CCCCTTCCTC CCTGCTTCTC CGCAGTCCTT CCACACCGCA GCCAGCAGCA 900
TAGTTGTGGA TGAAAATCGC ATCCCTCACT CCCTCACCTA AAATCCTCCA GGGCTGTCCA 960
TCCGCTCAGC ACAAGCCCCA GGTGCCAGCC CTTGTTCTGA AGGCTCTGCA AGACCCAGCC 1020
CAGTTGAAGT CTTCAACTTG CTCATGCCAC ACCCTCCCCT CCGTGCCCAC CACCCCCTGC 1080
TCCAGCTGTA GTGGCCCGTT CTAGAAGACT TGAGTCCCTT TCCCACGAGA TCCCCTGCAC 1140
CTCGTGTAAT TTCTGGCACT TAATCAGGCT CCATAGATAC TGGTGGGATA AATGAATCTA 1200
CCTCGGACTG AATGATGGAG ACAAAACATA AAATCAAAGC CGGGCGCGGT GGCTCACGCC 1260
TGTAATCCCA GCACTTTGGG AGGCCGAGGC 1290
|
