| Tag | Content |
|---|
EnhancerAtlas ID | HS133-31675 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr9:38380280-38382660 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Rhox11 | MA0629.1 | chr9:38381931-38381948 | TCCTTTAACAGCAGAAT | - | 6.01 | | TBX21 | MA0690.1 | chr9:38380620-38380630 | TTCACACCTT | - | 6.02 | | TBX2 | MA0688.1 | chr9:38380619-38380630 | TTTCACACCTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_01762 | chr9:38380680-38383801 | Aorta | | SE_28948 | chr9:38378684-38384162 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr9 | 38380317 | 38380552 | | chr9 | 38380679 | 38381519 | | chr9 | 38381534 | 38381667 | | chr9 | 38381693 | 38381840 |
|
Enhancer Sequence | CTAATATGTA GCCAGCACCA AGCACCACCC CTATCTCTCT AAATCTGTTT CCTCCTCTAA 60
AATAGAAATC AGTGTTAGGT TACCCCACGT GGGTGTGATG AGCCTCAAGT AAGGTAATCC 120
CTGTAAAGTG AGTAGGACAT AGTAAACCAC CAATTCATTA CTGTGACTCA CGACTGACTC 180
CCTGTGGATG TGCAGTGGTC CTTTTCCCTC TTGGGTCTCA GTATCCCCAC CTGTACCTGG 240
ATCATCTTTC AGTGCCTCCT GCTATATCCC CTCTTATGAA TAGAAAGATT CAGTAGATCA 300
CTTACTCAGT GACCTTTTCA GGTGCACTAA AACCAAGCAT TTCACACCTT AGGGAGACAC 360
AAGGCAGGAT CTAATCAGAA CTCTGCATCC CTCGGGCTTG GTTTAGGGAT TCTAGTGCCA 420
CATTCAAAGC ACAGAACAGG CGCCTGGGCC AATGTCACCT TGGTAAGTGT CTGCCTCCCA 480
GCGTGCCTTA AGGTTGCAGG AAATTGCCTA TTTACACGTA TTCTGCTCTG ACAGGCACAC 540
CAGAATTTTA AAATCCTCCT TCAGGTTTCT CACAGATAAG ATGGGGAACT TTGTTTACTA 600
TGGATTCCAG GGCTTCCTGA AGAGGAGGCC TTTGAGTTTT CGAAAATAAT TGCTTTTCCT 660
CTCCTGTGCT CTCCAGGGGT GGTCTTTGGC CGGAGGAAGA AATGGCTTTG TTGCTCAGGA 720
GAGCTTTGGG AATGGAACTC AGGGGCTTCC AAAGAGCAGC AATCAGGAAA ACAAGCAGGG 780
AGGATCCAGG TTTTGCAAGG CCTGAAGCCT GCACACTAGG GAGCCCCATG CTCTGTGAAG 840
GAGAGAACAG TGATAAGAAG AAGATAATGA TTCAGCAGCT TTGCAAACAT TGTTTGGTGA 900
ATAAACAGCC CCGTTCAGTG CACCGGTTTC TTCCTCCCAT CATGGGACAG GTGGAATGTG 960
ATCTGAGATG CCAGCCTTGG TCAGCTGGAG GGTTGTTCAG CTGCCTCGTG ACTCCTCCTC 1020
GGTAAGAGTG AAAGAGCCTT TCATTCCCTA AATAAACATG TCTATTAGAG GCATTGATCT 1080
GTCCCCAGCA GGCAGTAATT GCACCTCAAA TGCCACAGAT GCACAGCCTG GGGTTCTACT 1140
CCACCCCGCC CTGCCCTGCC CTGCCAGTCT CCCTGCCTGG CCTGGGACGG ACCCTGACCC 1200
TCCTTGGGGT TCAGGCTCTT CTTCTGTACA GAGTCACAAG GCTGTTAATT CATATTCTTC 1260
CCATCACAGG GATGAACCCC TCTGGCTCAG TCATAAATGA TAATATAAGA CTCGTTTTCC 1320
ATGGAAAAGC CCTAGTACAG CCATACGGGT ACTTTAATAC AAAATGCTCA CCTACCAGTT 1380
TGTAAGCAGC CCCTCTCTGA GCCCCTAGGT GCCACCTCCA CTCTGTCCTC ACGGCCCTTG 1440
GCCTGGGACC CCCTGAACTT CCGCATGACT CACCATGGCC AACCAGATCA CAAGGGTTAG 1500
GGTTAGGGTG AGCACAGAAT TACAGCCAGG CTTTGTGCCC ATGCTCCATT CCTCAGTATA 1560
TCAAATCTCA CCCCTGGGCC TGGGCTGGGG CCCCTGCACA GGCTCCAGCC CTTCTTAGCC 1620
TAGAGAGAGG CTTCTTGAGG AGATTCTCCC ATCCTTTAAC AGCAGAATCC AGCCTGCCTG 1680
GATTCACTGA ACAGGAGTGC AGCTGGGAGT GGAGCCATTT CTGAGCCGGT GAGCCCTGAT 1740
CTGTCTGCTT CTACCTTCAT TTCTAACAGG TATTTCTGGC CCAAGAAGTT GGGCCTGGGA 1800
GGACAGACCC AGCCCAACCA TCCTCCTGTG AAGGACCCTT CGTGACGGGG TGGAGGCCAC 1860
ACTCTCTGGC TCCTGCTCCT GATCACTTTC CTTCCCGTTC CTCATGAACA TGTCCAGGCA 1920
TCAGCCCAGG GGCAGATCTA GGAAAGCCTG GAGCCACCGG GCCCCTTGGA GCTTCCTCAG 1980
GGGCCACCAG AGGGTGGGGG CCCGGTAAGC AGCTCCCTTG CACCTGGCTT AGTCTGTAAT 2040
CTAGTGCAAT CCCTTCACCG TGAGGATAAT TGGGCCCAGA GGGCTCATGG TGAGTCAGAC 2100
AGCCTGGGGT CCAGTCCCCA GCTGGGGGCT TTGCCCACAG CACCTTGTGC CCTCTCTCCT 2160
TTGTGGGTCT ATCCTCGTCC TCACACACGT TGTCTCTCTG TTCCAGGGAA GGAGTATTCC 2220
ATGGCCCATA ATCCGTGTGA ACAGATAGAC AACGGGAAGC ATCTTTGTTA TTCCAACACT 2280
GGGGCAATTT CTTTCACCAA CCCGTAGCAG AGGCCTTAAT GAGGCTTCAG TCTAGCTGAA 2340
AAGGTTGTCC AAACCCCACA CGTAGCACCA GGTGAGCCAT 2380
|
