Tag | Content |
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EnhancerAtlas ID | HS043-23288 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr2:106732260-106735020 |
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) |
NR2F1 | MA0017.2 | chr2:106732299-106732312 | CCCTTGACCTCTG | - | 7.34 | STAT3 | MA0144.2 | chr2:106733234-106733245 | CTTCTGGGAAA | + | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35803 | chr2:106730896-106732976 | HepG2 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I106114 | chr2 | 106731166 | 106732963 |
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Enhancer Sequence | TTATCTACCT CCAAGGGATG GTTCTCAACC CAGTAATTGC CCTTGACCTC TGTCCCCAGT 60 TTTCTGATGA CACTAATTTA CTTTGAAGTG ACAGTGACCA CGTGTGGAAT AGCTCACAAA 120 CATTGCCACA AGGACACTAG GATTGCAAGG AACAGGCTGA GGCTCCCAAA GGCCCTTTGG 180 AAACACGAAC TAGGCTGGAA CAGTGTAACT GGCATCAAAC GCCTCCTTGC CTCATTCGTA 240 GCAGCTGAGA GAGGGGTGAG GGCTTGGGTA TGCAGGTCCT GAGACGTGGA GCCAACTAAC 300 AGCAGGCCTG ACAGGCAAGA GGTGACCCAA GAGGAGTAAT GAAGGTACAG GGATTCCTCC 360 CTCCCCAGAT ATCTCCCAAG GACAGAAATG TTACCAGCAG GGATTACACG GTGTACAGAG 420 CACCTCTGAC AGAAGTGATT TTATCTTAGA AAATGACTCC ATTTCACATT TCAAAAGGCA 480 TCCAGCCAAC ACGGTCCAGA TATTTGCATA ATCAACAGAG ACAACACCCA ACCAGATTAA 540 GGGCATAACC CTTTACTGTC AGTCCTCACC AAAGGACTCA AGGGCGGTAA TGAGCAGGAC 600 TTCTACAACT CGAGATGGCC ATCTTGACAG ACTCCATCTT GCTGTCACTC ATGATCAGCA 660 CCCAGCATCT GCCGCCAAAG ACTGCCCAAA TCAAGGGCTC TTCCATGCAA GATGATGCTG 720 CCTGTCCAGA TAAGCCCAGG ACCCTCTCTT TGTCCATGTC ACTGTCCTTG GACTAGTTCA 780 TTAACCCCTT TTCCTCTCCC CGTGTCTCTT GATGTTAAAT GTTACTCTGT TTGATGTGGA 840 CTGCTTAATC TAAACATTTA TATATTAAGT ACACTACTAG GTATGGTTTG CAGTACTGAC 900 TGAGCTGTGG AGTGGCTTGA GCCTGTGTGA CCACAGCTCT GATTACCGAG TGAATGGAAA 960 ACACTAAGAA GTTCCTTCTG GGAAACTGCA TGGAGCACAT GGATTTTATG ATGGAAATAG 1020 TATCAATAAA AGCCTGACCT TGTGGAAAGA CACAAACGTT CATGGACCTG GTTATGTCTG 1080 ACCTTGCCCT GCTCACGACA CATGGGTTCT CCCTCAAAAT TTCTTTTAAA ATGCAACCAT 1140 TCAGTGGAGA GTACAACAGG TCCCCAAATA ATATCATTTC ATGATAATAC TGATGAGAAA 1200 AAAAATCACC TCCTGGCTGG GGCTACTGTC TGCACGCAGC TGGCATGTTC TCCTCTCCCC 1260 ACGTCTGTGT GGGTTTTCTC CAGGTATTCT GGTCTCCTCT CACATCCCAA AGCTGTGCAT 1320 GTCAGACAAG TGGGCTGTTC CAGTGGTCCC AGTGTGAGTG AGTACGCCCT GTGAGAGGTT 1380 GGCATACTGT CCAGGGCAGG CTGCTGCCTG GAACCTGGAG CTGCTGCGAT AGGCTCTGGC 1440 CACCTGAGAG CCTGTCAATA ATTATCTTGC TTTTATTAAT CTTCCTTAGG TGGATAGCTC 1500 ACATTTATTT CAAATCCTTA ATATTAGAAG TGTTTTAGTC TTTATTTAGA ATTTTGGTGA 1560 TGTTTTTGTG ACCAGAAATA TGCCTGGGAA CTTAACTCTT GTTATAGCAA TTAGCCTGTG 1620 GTACTGCTGA TTTTGTTCTA TGTCCTTCTG CTTAAAGTAG CAGTTTCCAA GAACCTGCTG 1680 ATGGTGTTAA GTGATGACTT ACTGTGCTAT ATCAAGCCAC CGAACACTGT AACGTGATCA 1740 CTATATTCGC TGACGGAAGG TTCTATTGAT AGAAGGTGGA ACAGAGCCCT GCATAGTGGG 1800 AGCAGGTCCT GAAGGAGGTG CCTGGGCATA TTCACCTGTA GGGAATGGAA TGGAGAAATG 1860 CCAGGAAGTG CACCAAGGTA CAGCAGCCCA GGCTCTCTCT GACGCTTCTC TCAGAGAAGT 1920 ATATGCACAT CCCTAAAGCA ACGGAGTCAG GCTGTGAGGG CTGAACCCCC TAACTCCCCT 1980 AGGGCCTGTC ATGCATACAT CTCGATGGGT TCTGCTCCCT ACCTGTGGAT AAAACTAAGG 2040 CGACTGCAGA ATGCACAGCT CACTGTGCTG AAGCACGATT CTCAAAGGTG CTAAAAGGTT 2100 CAAGTTGACT CGAGGGGTTG GCTGAGGAAG GGGGTCCAGG AGGGGTGTGT CTGCATCTGT 2160 TTGGCCATCT TCCTCAGCAC TCCTGCTTCA GCATCAACAA TCAGCTGACC TTCCTGAGGT 2220 TTGCTCTGCA GCAGGCCAGG AGGGGTGGAT ATCACTCTGC CAGTGTCTAG GTGGGACACC 2280 TGGGATGTGG CCAGCAGGCA CCCAGTGAGT CACAGGGCCA GGAAGCCAAG CTGCTACTGG 2340 GCAGGTCCAG AGGACAGGAC GGGCCTCCTG GGGTGTGAGT CCTAGCCATG GAACACTGCA 2400 CCTGGTTTGG CTGCTTACTT TTTTTTTTTT TTTCCAACTC AGGTAGAATA TATATACCAA 2460 CTCCGACTTT TTCAAAAGTA CTTTGATGCC AGGAACTAAA ACAAAACCAT ACCTTCAGGG 2520 CCATTAGACT AGGTGATTTC TGAGTTTGCT TTCTTTCCAC TCTGCCATTT GCTGGTTTTA 2580 TGAATGGAGG CTTGTTTTGC AGATCCAGCC CAGTGGGTGG GCCACAGACC TCAGAGTCAG 2640 ACTCATGAGG GGGCGAACTC AAATGCACAC TAAGCACTGA CCGCAGCCTA CGGGAGAGGC 2700 CCCCACATTT ATCAAGCCAC TGAGTCCAAA TGCACACAGA GGCGGCAATT TAATTCCTCC 2760
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