Tag | Content |
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EnhancerAtlas ID | HS133-27816 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:2262390-2265040 |
Target genes | Number: 20 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr7:2262911-2262931 | ACACAAACCACAAACCTCCA | + | 6.03 | RUNX1 | MA0002.2 | chr7:2262915-2262926 | AAACCACAAAC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | TGTTAAGAGA GCAAGAGTCA GATGCCACGT GCCGCCCACG GGAGGGTCAG CGGGGAGCCC 60 TCACCCCCAC ACCTCTCTCA GAACATGCCG AGGCACAAAA AAGAGCCGAG CAGGACCCAT 120 GAGCCAAGTC ATAGGCAGAA CCAGGACGGG ACCTGGGACC CAGCCCCAGC GTTGGCACCC 180 CCGCTGTGGC ACCATGACGG TGAGCACTGT GCGAGGTCAG GGCTCCCAGG AAGGGCACTT 240 GGCACAGATC ACACACACAT TTATCACACC GTCTGCTCAG CAGTTGCCTC TGCAGGGAGA 300 GGGGGCATGG GAAATCTAAA ATTCAGCATT GACCTTGGGG AGAAGCTGAG CTTTCATAGC 360 ACCAGCAAAT CCTGTCTAAT TACGCTCTGT CCGGCACTGA AAGGAGCTGG CACTCCCCCA 420 GCGAGCAGAC AACAGGGGCA GAGACAGGCA GCGTGGACAG GAGGCTGTGG GCAGAAGCAG 480 TTTACACTGG GCTCAAATCT GCCACACATG CACCCCCTCT CACACAAACC ACAAACCTCC 540 AGACCCACCC CCCACGACTG GCCTTAGGGA GGCCGCGTGG CTCTCACTGG TTGGGATGGG 600 ACATGACCAA GCACCACGCT CAGACCTCCT GACTCTAATG ACCCGCAGGC CCTCCAGAGT 660 TCACTGCCAG GTACCGGCGT CCCAGGAGGT GAAGGCGGTG AGTCCTGGTG GAGCCCGGCA 720 CTCCGGGACC CTCTCACCCT GCCTTCCTCG GGAAGCACCA AGCACTCCCG GAGCCCCGGG 780 TGGAGTACGA GCTTGTGCTG TCCTCATCCA GGGTACTCCA GCCCAAAACC CAGGAGAGCT 840 GTGACAGAGG TGGCCGCCTT CTGAGAGAGG CTGACCCGCG CACCTCGGAG GGACTCCAGC 900 CCTTGTGAGC TGCAAGGGCT GCCTCACAAC AACCAAGAGA CCCTTCTGTG ATGCAGGACA 960 AGAACTGGGG TTGGCACGGG GCTCCGCTCA GCACCATCAC AGCCAGATGC GGCACCGGGC 1020 CTGGAACTGC CAGTCCCAGC GCAGACAGGG CAGCCAGCAG GTCTTTGGAC TTCAGACACT 1080 TAAGTCTCGC CCCTAATAGG TATTTCCAGG TGGAACTCCA AGGAACAATT GGAAAACTAC 1140 TGGTTCTGAC TGTTCCTGGG GTCCCATGCA GCTGTGTCTG CGGGCAAGGA AGGACAGTCC 1200 TGTTAGAAGG TGGCTGGAGC TCAGCAGGGA GCCCCAGGTG TAAGCCCAGT CACCTGCATC 1260 CTTGGATTTC CCCAAGACAG GGTTCCCGGA GACCCTACAA TGACCCCTCC CTCAATCCAA 1320 CATTTGTGAG CACCCATAAA ATGCCATAAG CTGTGCCACA CAATGGAGAT CCTGGGCAGA 1380 GTCGGGTGGG CCCTGCCCTC AGGGACTCTC GGCCTAGAGG AACTCCAACA GCTGCACACT 1440 GTCCCTCCTG CCTGACAGCC ACAGCCATAC CATCAGCATG CTGCCTCCAG ACCAATGACC 1500 TGGTGGCTCC TCTCCACCCC TAACAAGGGA ATCTCAGTAG TTAGGGAGAC TCCTGTGGAC 1560 TCTCCCTCCC CTTCCCACCA ATTCCTCCAG TACTGTCCCT CCTAGGACCC ACCCAGGCCA 1620 TGAGCAAACG CCCCACCTCT CAGGGAAAAC AGCTCTCAAA GCAGCAACGG AGCCAACCCT 1680 GAGGCAGTGG CCCCCACCCC AGCGGTGCCT CAGTCTCACT GAGCCCACAC AACGCACACC 1740 GCAGTCAGGA TCTGCAGGCC AGGGGCAAGC AATCCAACCA GCATCACACC CCGGAAGACG 1800 TGAGCTATTT TTCTAGGGCC CAGGAGAGTG TGTGAATACA CCGCATGATG TCAGGGCGGG 1860 GCTGGACATC CACCCGCCAA GAGAGGGCAC GGAGGCCAGG GAGACTTTCC GCCCAATACT 1920 CTGCCTGAAC CTTGGCAGCA TTTCCACAAC TGATCAGCAC TGACTGAAAC CCTGGCAAAG 1980 TGCTGTTAAT CAGAGCAGAG GGGATCCGCG CACTCAGTGG AAACCTAATT CCCTCCCCAA 2040 GGACAGGGTG TTTTCCCTGC TGCCCTGGGG AGCCAGGAGC AACACAGAGC CGCCATTGAG 2100 ACCGGCACCC TTTGCTAGGG CCCTCCAACC CCAAGACCCA GCATGGACCC GAGACCCTGA 2160 TCCACCCCAT GACCTCCTAA GCCTGTCACT CCTACACCAC TTGGCATTTC TGCCAGACCT 2220 GCATTCCAAT TCTTCCAGAG GGAAGAGGAA ACCAGGAGAC CCAGCAAAAG AATCTGTGCC 2280 AGCACCGCAG CCTCAATGAA CAGACACAGC AAGTGTTCCC ATTTCATGCC ACCCTCCTCT 2340 AGGACATCAA GCATAACTGA TACCTGCCCC ACAGCATGAG TGGCCTCAGA AGGAATGTCC 2400 TGGCAACCAT GACACAGGGC GTGTCAGGCT TCCAGCCAGC TGGGTTCTCA TTTCCTACGG 2460 CCTGGCAGGT ACCGTGCACA GCCCCCTTGC TCCCAGGGAC TGGGATCTGA TTTCTTAAGA 2520 CCTGGCAGGT ACCATGCACA GCCCCCTTGC TCCCAGGGAC TAGGATGTGA TTTCTTATAA 2580 CCTGGCAGGT ACCGTGCACA GCCCCCTTGC TTCCTGGGGC TGTCTGGGCC GACCCTCGCC 2640 CCGCCTGAAC 2650
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