| Tag | Content |
|---|
EnhancerAtlas ID | HS133-29144 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:99677410-99679250 |
Target genes | | Number: 43 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gabpa | MA0062.2 | chr7:99678659-99678670 | CCCACTTCCGG | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCTAAGTTCA AGTGATCCTC CCAGCTCAGC CTCCCAAGGA GCTGGGACTA AAGGTGTGCA 60
CTGCCACATC TGGCTGAGTT TTTTAAAATT CTTTTTGTAG AAATGCAGCC TCACTGTGTT 120
GCTCAGGCTG GTCTCAATCT CCTGGCCTCA AGTGATTCTC CCACCTCAGC CTCCCAAAGT 180
GCTGGGATTA CAGGCATGAG CCACCGAGTC CAGCCTAAAC TTCATTTCTA ATCAAGACAT 240
TTAAAGAAAA GGAAAAAAAA GAGAATACTT ATTATATGCT AATAAATACC AATTAAGACC 300
ACCACCACAA CTAGTATTTG CGTTGCACCC GTGGAGAGAT GAAAGGGAAT GGTAGGTTCT 360
CAGGTCCACC TCCACCCAGG GTAAGAAAGT TCTAACGTTC TGTCAGCTAA CTTGCTAGAC 420
ACTGTGCTCC GAACTACTTC AGCAGGGGAT CCACATTGCA CAGCTGAGCC ATTAGAAGTC 480
TTCAGGTGAT TCGCTGAAAA TCTATCTCCT TGGACCTTCA CCGCACAGAG ACCTAGTGCA 540
TCACAGAAAT TCAATGACTG GCGACCTGCA GTGGCTCACG CCTGTAACCC CAGCACTTTA 600
GGAGGCTGAG GTGGGAGGAT TACTTGAGCC CAGGAGTTCC AGGCTATGGT GAGCCATGAT 660
GGCACCACGG CACTCCAGCC GGGGGCAACA GAGCAAGACC TTAATACACA CACAAACATT 720
TTAAAAGGAA AAAAAAAAAA AAGGCCGGGC GCGGTGGCTA ACGCCTGTAA TCCCAACACT 780
TTGGGAGGCC AAGGCAGGTG GATCACTTGA GGCCAGGAGT TGCAGACCAG CCTGGCCAAA 840
AGGGCGGAAC CCCGTCTCTA CTAAAAATAC AAAAAATTCG CCGGAGGTGG TGGCGGGCGC 900
CTGTAGTCCC AACCACTCGG GAGGCTGAAG CAGGAGAAGC GCTTGAACCG GGAGGCGGAG 960
GTTGCAGTGA GCCGAGATCG CGCCACTGCA CTCCAGAGAC AGTCTCAAAA ATAAATAAAA 1020
ATTAATTTTT TTAAAAAAAG AGCTTCAATA ACAGAATCTT CTCCTTCCAC CCGACTGTCC 1080
ATCAAACACG TATAATCAAA TGATGCCCAC TCTCCACAGA TGTCTTTTCT GGAGAAAATA 1140
ATACGCTCGT TCCTCTAATT AGCCCATCGG TTTCAGGTTC ATCACTCTGC TATCTTCTCC 1200
TGGAGTTTAC AAAAGCCCTT CAGAGTGTAA ACACCGATGT GGATTCAATC CCACTTCCGG 1260
AGAGAGGATC AAACCAGGAA TCTAATACAA CTGAAAACGG AGCCTGAGCC AGGTGTATCA 1320
CGCGATGCAC TGGGCTCCAG CAGGATTACC CCTGGAATCG GCGTCTGCAC CCACTCCCAG 1380
CCCTCGTGCT AACTGCGTAC GCTTAGCAGA ATTTCTCTGA TCCTTGGACC CAGCTGCGTA 1440
AAAATAAACT TCCTCTCCTG CCACGGGCGC GAATAACTGT GTTAACATCA AATAAAAACG 1500
TCTGGGAGAA ATACCAAGTT AGGGTCGCTG TCATTAGCTG CTTTCAAGAG AGAGGCGCCC 1560
CTACCGCTCT GCTGAAACTT TTAAACGCTC CAGCTGGGTC GCCGTTAAAG TCACAAAACC 1620
AGAACCGGAG CCCCATTACT AACCCCTACG CAGGATCCCG CTAGGCTAGG GGGATCCCTG 1680
GGGAAGCGGA GTAGAGGACG GGCTGCAGGG GACGGAGGGG CGCCTCCCCG AACCCTGCTC 1740
CGGGCCGGCC GGGGGACCCT GCGGGCCGCA GTGGCACAGA CACCACCCCC TTCCCCGGCG 1800
ACCACAGCCT CCGTCTCACC GCGAGACCCG GGGACGCGTG 1840
|
