| Tag | Content |
|---|
EnhancerAtlas ID | HS133-29938 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:150600570-150601930 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr7:150600934-150600949 | ACTGCTGAGTCACAC | - | 6.67 | | Nfe2l2 | MA0150.2 | chr7:150600936-150600951 | TGCTGAGTCACACTG | - | 7.35 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 150601112 | 150601617 | | chr7 | 150601662 | 150601810 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I150903 | chr7 | 150600499 | 150601798 |
|
Enhancer Sequence | TCTCTCTCCA TACCTCTCTC TCTCTTTCTC TGTCTCTATT TGTCCCTCTC TCTTCTCCCC 60
CTCTCCCCTA CCCCCCTAAG CCTACCGGGC GGGGGGCTCC CTGCTTCTTC CCATCCCACA 120
TCACCCCTCC TGGCTTTCTC AGCCCTCTTG TCCTGCAGAT TTTGTGGCCT TCACACACTC 180
GCCACATTCT TGTTCCACCG TGGCACTCAG GGTCTCCATG GCTACCTATG CCCAGAGCTA 240
AACAAAGCGC TGGTGTAGCT GGGCTCCAGC CAGGGCCCAG GGTGGCAGGC CCAGGACCTC 300
CAGGTGCGGG CACTGTTTCC GCTGAAGCGG CCGGGCCACC GCCAGCTCTC TTGGCAGCCT 360
TGGCACTGCT GAGTCACACT GGGCTTTCTG TTTCCATAAA ACATGTTTCA GAGATTTATG 420
AGGTAATCAT GTGCTCACTA CAGAAAAATT CGAAAACACA AATATAAAGG ATCTATTTCT 480
CCTCGGTCTT TTACTTATGC AAATTTTAAA ACAAACGTCG ACTTAGTCTA TATATAGCTT 540
TTGCTTAACT TCTTATCAAG AGCATTTACC CTGCTCATAA TGTGTGAATG ATATTCGTTT 600
ATGGATTACA AATACAATAG CGGACAGTTA TTACTCTGCT GAATACTTTT TGCTGGCTAT 660
TTTATTTAAC AAACTACCAC GTGGTTTCCC CAAGAACAGT TAGATTCCCC ATTTCACAAA 720
TGTGGAAGCT GAGGTTTAGA GTGGTTGAAT AAATTGTTCA CAGTCACACA GCTAGTACAT 780
GGCAGGTCCC AACTTTGAGG CCAAATCACC TTGTTTCACA GCCAATGTCA TTTCTCTCCA 840
TGACCCCTCC TGCCTGTGTA CCACAGGTCA CAGGTGTGCA TGAGGTGTCT GTGTGTCACA 900
GGAGGGCATC ACCACTCTCC TCCACCTGGG CTGAGCTATG TCCCTCCAGG ACAGTGGTGG 960
AGGATGCTTC CCAGGAGGAG TGACATCCTG TTTGTAAGCC ACCAGCTTGT AAGTCATGGA 1020
GTTGCCTGTG GTGGCATGGC GGAAGCCTGG CTGTGCTCTG TGGGCCAAGG GCATGAGGGA 1080
CAGGCAGCCC TTCATGGCAA AGAGCCAAAG AGTAATTCAG AAAACTAGAA TTTGAATAGA 1140
ATCACCTCAA CTTTTAAAGA CGGCATACCA AAACCCCAAG CAAATATCAC ATCCAATGGA 1200
GAAACCTTAG AAACATCCCC ATCTAGATTG GCAAGAAGAT AAGGTGCCTG TTAGCATTGC 1260
TGCTATGTAA CAAAGAGCCA GAGTCAGGGC CACTGTTATA AAACAAGAAA AGGAAATGGG 1320
AGGTGTAGAA GTCGGAAGGA GGAAAGAGAT TAAAATGTTA 1360
|
