| Tag | Content |
|---|
EnhancerAtlas ID | HS133-01608 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:47076800-47078140 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr1:47078010-47078023 | TTCTGGAAGGTTC | + | 6.19 | | RREB1 | MA0073.1 | chr1:47077911-47077931 | CACCCAACCACCAACTCCCT | + | 6.44 | | TBX20 | MA0689.1 | chr1:47076861-47076872 | CTTCACACCTT | - | 6.32 | | TBX21 | MA0690.1 | chr1:47076862-47076872 | TTCACACCTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCTTCAAATA TTCAACAACA CGAAGAACCT TCCATTTATG AGCAAGGCCT TGTGCTGGGC 60
CCTTCACACC TTTTGCCTCT AATCCTTAGA ACAATTCGCC TGATGTGTCT GATTGTCACT 120
TTAGATATGA TAAAACAGAA GTGCTTATAA AGGTGAAGCT GCTAGCCCAA GGCCACATAA 180
GTATTAATCA GTGCAGAATG GAGACTGGAT TCAGACCCTC TTTGCAGTGC ACTGCAGCGA 240
CCCTCACAGA TATTGGGACC CATGAAAAAG GCCCCGCTTC TGCATAGTCC CCCATGCTCA 300
AGGCAGAGAT CTTGGTGGCT TATGCCCTCT TCTCTGTGTG GCAGTCACCC AGGGTTTTAG 360
GCATCGATAC CTGGAGTCCC ACAGGCCCAG GGAGGTATGG CCAGCAGGGA CTATGAATCT 420
ACATTCAGGT CCACAGCTGG CCCACCCGGC TCTGTAGACC CCCTCCTCTT CCTCACCATT 480
CCCAGGTGGG GTCGAGCCTT CCCTCCCTCT GAGCCCCTCC AGCCCAGCCC AGATTCCTCA 540
GACATATCCT GCCCATGTAG ACTTGGGGTC CTGGGCTCCC ACAGATCTGA GCCCCAGTTC 600
GGAATTCCTC CCAGTTCAGT GCACTTTCCC TCAGTAGCCT CAAGTTTCCT CCTATGTAAA 660
ATGAAGGTGC TCCTTGTCGG GCATGACAGT GCAAGAAACA GCAGGCCACT GGCTGGGGAG 720
GAGCCGTGGG CATTGAATTG TGACTCAGTG CCCAGCTTCC TTCAGCATTC AGACTTCTCC 780
CCTCAGGGCT TGACCACCCT GCCCCACCCA CCGCTGATCC ACACAGCCTC TGCAGAGATG 840
AGCTCCAGGC CAGGTGGGGG CTGGGCCCAG CTACAGGTGC GGCTGGTGTG ATGAACACAG 900
TGTCATGCCT GCTCAGCTCC TGGACCAACA ACCCCCTCCT GCTGCCCTCG GGTGGGTAAG 960
CAGTGCCTGG GTGACATCAC TCATCTCCCC TCCCTACCCT CACCCGCCCA GGCTGCCCAG 1020
CTGAGATAAG AAAAGGCCCC ACAGCCTGTG CCTGGCAAGG GAAAATTCTG TCCTCAGAGC 1080
CCCAATCTGA GGTGATGATA CCACCAGGGC CCACCCAACC ACCAACTCCC TCCTTTTCCT 1140
GAGGCCAGGA GTCAGAGGGA ACCCCGGGAG GCTGGAGGTC AAATCAGCTA TGAACACCTC 1200
GGGGCAACTG TTCTGGAAGG TTCTGAGAAT CACAGCATCT GTGGTCTTGC CAGAGTGGTC 1260
CTTGGTGGGA CCACTTATGC TTTAGAAAAG AAAAGCCCTC TGAGGTGGGT GGATCACCTG 1320
AGGTCAGGTG TTCGAGATCA 1340
|
