Tag | Content |
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EnhancerAtlas ID | HS118-09497 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:8444790-8447180 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr2:8445165-8445180 | ACATGACTCAGCAAC | + | 6.76 | Nfe2l2 | MA0150.2 | chr2:8445163-8445178 | CGACATGACTCAGCA | + | 7.2 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_20349 | chr2:8440084-8447022 | CD56 |
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| Number: 2 | ID | Chromosome | Start | End |
GH02I008305 | chr2 | 8445131 | 8445930 | GH02I008306 | chr2 | 8446550 | 8447641 |
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Enhancer Sequence | GTAGGTATGC TTTAGGGGAA GAACAAAAAC AGACAAGGGC AGTGGGAGTT TTGATTAGCA 60 TAATCTTTAC AAATCCTTGC TTTGGAATTC CAGCTTGGCC ACCTACTACA TCATTTGGGC 120 AAGTTTCTTA ACCTCCCAGA ACCTCAGTGT CCTCATCTGT AAAATGGCAA TTATGAGAAC 180 GCTACCTACT TCATCACAGT GGCGTAAAGA CTTACTAAGA TAATTCCCGT TAAGTGCTTA 240 GCACGTCGCC CTCCAAGCAG TCTGTTATTT TTCTGATGTG TCAATGTCAC CATTCACCTG 300 CTGTGCAGTT TTGAGCAGAT GATGAACGCA TGTGTCCTCC AGGAGCTCCT TCTGCGACAT 360 CCCCTAGGCA GCCCGACATG ACTCAGCAAC ACGGTGCTAG GGCCAGATCC CTGGCTAGAC 420 ACCGAGGTGT GGGGCCCTCG TCTCTGACCT GCCATTGAGC CACAGTGTGA AGCCTAAGCA 480 AAGCCATTTC TCTAGGGACC TTGGCTTAGT TTTCTGGTAA AATACAAGTT TCATTCTAGG 540 TGTTCTCTCA GCTATCTTCT AGGATGTTTT GGAGTCTGTG CTTTCATACA AACACAGGCT 600 CATGCTGGAG CAGGGATGGC CATGGACATC CTTAACTCTC CTAAGAGCCA CCCACGGCCT 660 CCCAAGTCAC CTCATCAGTT GTCCTCACAG GGAGCCACCC TCTGGGAGTA TTTATATCCC 720 TCTACTTTGA TTACAGCTGA TTAGTAAATT TACAATGTGT TTGAATTTCA CTAGACTTAC 780 ATTTCACAAC AGAGAGCAAG GTTTAGTCAA CACTTTCATT TGCTAAGGGC AACCATCCAG 840 GCTTAATAAG GCTTTCCCTA AACAGACACC TTCTTTACAA ACTTCTAGGA AGCCAAGTGT 900 TAAACAAAAG TCTAACTTGA GACTTTTCTC TTGATTCCTA TTATGGGCAT TTGCAGTTTG 960 CTTTGCAATT GCATTACCAA GTGCACACTT GCGCACATGC CTGGAAACGT GCACACACGC 1020 ACAATGGAGC AACGTCCCAG TGTGACGGTT CCTGCTGGCC AAGAACAGCA CTGGGTATTT 1080 GCATGGGCAA AGACTTTAAC AGCGTGAACA GGATTTTCTG AACAAGTCTG GAAATAAAAT 1140 ACCTACCAGC TTTCAGAGTA AATTACCAAA AAAGCAAAGG AGAAAAACAG TTCTTCCAAA 1200 AGACAGTCAT CTAACCTCCT TACTCCCTGT GCACAAATTA CCAGGCTTCC CAGAATCCAA 1260 TCTTAGGTGA GATGAGGAAC AATGGAAGGT ATTTACAAGT TTAAAAAATA TCAAATTTTT 1320 GCTTCTGGAC TCCCATGCTA TGATGTCACT ACCTTGTTGC ACTGGTCTGA GAAAAAGAAT 1380 TATATCTCTA TGGGCCTCAG TTTCCCTGTA TGTGAAATGA GAGTTTCAAT TAAGCACTAT 1440 CTCAGATCCT TTCTGCCTTC AAAATCATGG GAAATCTCTG TAACAGATTT TTTAACCCAT 1500 GAGAGGCCTT AGGGTCACTA TGAGTATCTG ATAAACAGGT GGGCCTTCCC TCCAGAAATA 1560 TAGACAAAGG CTCATAAACA CAGAGAAGTT TACACAGAAT GTGAAAGAGG ATTCAGAGAA 1620 CCCCTGAAGC CTGTCCCGGA GGATGGGTTT AAAACTCTCA ACTCTGGAGG AGATGTTGAA 1680 AGACAATTTC TCCAAAAGAG AGGGAGAAGA TACAGTAGCT AGGGAAGTCT GGAAATCTGA 1740 ATTTTTAATT TAGAAATAGA TATTGTGGTT TTGTTGTGAG CTTTGAAAAA TTGAGCCATG 1800 ATTCTGTATA ACGCCTCTAA GACAAAGATA AGATGTTAAA GCAGGTTCGT GACCATGGTC 1860 AGCTATGGAA GCGGTACACA AGGCCAGTTA GCAGGGTGGA GTCAGGTTCT GAGAGATGAG 1920 GTGGTATGGG AATGTCTGGG GCTGTGGGTA ATAAGTTGAG CTTTTTCCCA GATGTTCTCT 1980 CCATGTTCCA GAGAAGGTAG AAAGCTGGCT ACCGACCAAA TCTGATTTTG ACATTCCTGT 2040 AAGATAGTGC CAAGCACTCA GATCTCATCA GCCCCGTGTC AGAGGCAGCA AGGCACCACA 2100 CCATGGTTGG ATAACCCCAC ATTCAATCCA TTTTACTGAA AGCAGCACAA ATAAACTAAG 2160 AATCAGAGCA CTCAATGACT CATATCAGAG GTATGAATTG AAAGTCAACA CTTGTATATA 2220 ATCTAACTGA AGGAGAGTTT ATAGCGCAGA ATTCTCTCTG TTGGAAAGAA AAACTCCAAA 2280 TGCGTGTGTG TGTATATGTG TGCACACTCA CTATCTTACA CAGCACTGCT CATTCTAAGA 2340 AAATGAGAAA GGAGAAGAGA AAGCAACTCA AAACTTTTGT TTGATTTAGA 2390
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