| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00624 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:23157360-23159470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr1:23159451-23159464 | GAATGTTCTGGAA | - | 6.62 | | IRF1 | MA0050.2 | chr1:23157853-23157874 | TAGCAGAAAGTGAAAGCATTT | - | 6.19 | | IRF2 | MA0051.1 | chr1:23157857-23157875 | AGAAAGTGAAAGCATTTT | + | 6.29 | | SREBF2 | MA0596.1 | chr1:23157402-23157412 | ATCACCCCAT | - | 6.02 | | TBX21 | MA0690.1 | chr1:23158262-23158272 | AAGGTGTGAA | + | 6.02 | | TBX2 | MA0688.1 | chr1:23158262-23158273 | AAGGTGTGAAA | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 23157740 | 23157851 | | chr1 | 23158530 | 23159269 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I022824 | chr1 | 23151232 | 23159621 |
|
Enhancer Sequence | TTTATGCCAA CGGTCTTAGA TCAACAAGAA GCATTTAGTC CAATCACCCC ATTTTACAGG 60
TAGGAAAACA GAGGCTCCAA GAACGACAGC AGACATTTCA AATGTAGAAT GGCCAAGTGT 120
GTGGGTGTCA GGAAGAGGAA GCTAGATGAA GGAAGAGGGG TAATGCTCCA CGTTGACTAC 180
CAGAGTCTGA AAGTCTGAAC CTGGGATGCC AGGCAGGCAG TAAACCCAGG GGCTCCCCAG 240
ATCAACCCAG CAGTACTGAC TGCATCTTTG CAGGTCCACA CTGGCAGCCT GTACACTTTG 300
AAGAACAGCA GGTCCACTGG GGATGAAGGG CGGCTGCAGG GATGGTGATG GGCATTGAGT 360
GAGGTGATTT ATATAGGGCA ACTTACAGAG TGTCTTGCAC ATAGAAGGTG TTCAGGTCCT 420
GGGAGGTAAG TGAGCACCAG ATACAAACCC AGAACTGGGA TGGGGAGTGG CTGCCCCTTG 480
CTACCTCCCC CCTTAGCAGA AAGTGAAAGC ATTTTGCACA AAAACTCAGC TGTAGGCATT 540
GTGTAATAGC ATTGATCTAT CCAAAAATAT TGAGTGCCTA CTGTGTGCCA GGCAGCCTGT 600
GAAGCCTTTT GCGTGAATCC TCTCATTTCA ACCCAGGAAC CCTTACAAGT CAGTCTACTA 660
TTATTTCCAT TTTATGGATG AAGAAACTGA GGCTCAAGGA GCCTGAGTGG TTTGCCTAAG 720
GTCAAGCAGA GCAGGGCAGG AATCCAGGGC TTTCCAAATT CAGAGCCTTA ACACCATGCC 780
ACACTGTGCT GGCAGAGATA GCAAGAGTTG TTGGAGATGA TTATAAGGGG AGGGCCAAAA 840
TGATCGTGGG AATCCAATCC CCGTGGCAGT AGGTGGGAGA TGCTGACCTG GGCTTCCTCA 900
GAAAGGTGTG AAATGTTGAC ACCCTCCCCT TGGGCTCTTC AAGGGCTCAA GAGGGGCTGT 960
GTTAGGCTGG GCTGGAAACA GAGGGCTGAC CATCATGGGT TCCAGAGGGA GCTATCCACC 1020
CCCCTACCTA GCCAGAGGCA GCCAGGATTC CATTAACCTG ATTCTCTGCC CCACATAAAC 1080
CTGCAAAGGG AGCCCCTGGA GGGAGGGGTA CTGGGGAGAG GAAGAATTGG GCTTCCCCAG 1140
GCCCCAAATG GAGCAGCCAG TGGTGCTAGT TTCCTCTCTT GCAGTCCAGG AGGACCTTCG 1200
AGGCCCCTGG CTGTTTGAGC GGGGAATAGG GAGAGCGATG GAGAGCCAGA AAGTAGGGAC 1260
AAGAGACTCC AGGCTGGGGT GCAACAGCAG GAATAGCAGG AACAGGGTGC ACGTCATCAG 1320
AACAATGGGT CCTGAGTCAC TCTGTGCCTG CCCAGCCCTG CATGGCCCTG GGTGAGTCAT 1380
GTCACTTCTC TGAGCTGTGG GTTCTTCCTC AATAGTAAGG GCAAACCAAT GCCACCTCTC 1440
AGTGTTGCTG GGCTGATTCA CAATACCGGG CCTCAAGAAA TGGTGGCTGT TGCCAATGCT 1500
ATAATTTTAC AATCTTGACC CCATGTATCC CTTCTCAGCT TGCAAGCCAC ATTCATCCTT 1560
TTTCTCCTTG GAGCCTCACA ATACTTCTGC AAGGTGTCCA GGATTCTTAC CAGAGAGGTT 1620
AAGGGACTTG TTCAGAATCA CACAGCTTCT AACCCTTGGC CTGGGATGCA CCCCTAGTGA 1680
TTGTCATGGA GTGGGCCATC CCAGCCAGGC TACGCCACTC TTCTTCAGTC TGGGTGGTTG 1740
CTATTCCTCT GCCATGATTC ACGTCAGATG CCTCTTCCTC CAGGAATCCC TCCCTGACCA 1800
CACAAGAGCC TGGTTAGTAC AACTCTCTGC TTTCCCACAA CCTTTGAGAC ATTTATCAGA 1860
GTGTTTATCA GCAGTCATCA CAACCGTTAG GTGCTCCCAC CTAAGACTTT GAGGGTTCAG 1920
CCAATACTTT ATAATAGAAG AAGAGGGGGT ACAATAAATA TTTTGTTAAT GACTACAGCA 1980
CCTGTACAAA GGGACAGATA GGTGTCCACA GACTCACATG TATAAGTAAC AGTCATGCAT 2040
GCACAGCCAT GCACATGTGG CTTAGTGAAT ACACATGTAT ACAGACAGGG AGAATGTTCT 2100
GGAACATGAA 2110
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