Tag | Content |
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EnhancerAtlas ID | HS118-01659 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:212400510-212403540 |
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) |
EWSR1-FLI1 | MA0149.1 | chr1:212401139-212401157 | GGAAAGGAGGCAGGGAGG | + | 6.16 | EWSR1-FLI1 | MA0149.1 | chr1:212403030-212403048 | CCCTCCTCCCTTCCTCTC | - | 6.27 | EWSR1-FLI1 | MA0149.1 | chr1:212403274-212403292 | GGAGAGAAGGCAGGAAGC | + | 6.39 | EWSR1-FLI1 | MA0149.1 | chr1:212403008-212403026 | TCTTCCTTGCTTTCTTTC | - | 6.41 | EWSR1-FLI1 | MA0149.1 | chr1:212403026-212403044 | TTTTCCCTCCTCCCTTCC | - | 6.4 | EWSR1-FLI1 | MA0149.1 | chr1:212401131-212401149 | GGATGGAAGGAAAGGAGG | + | 6.51 | EWSR1-FLI1 | MA0149.1 | chr1:212401135-212401153 | GGAAGGAAAGGAGGCAGG | + | 7.18 | HNF1A | MA0046.2 | chr1:212402044-212402059 | ATTTAATTATTAATC | - | 6.32 | ZNF263 | MA0528.1 | chr1:212403021-212403042 | CTTTCTTTTCCCTCCTCCCTT | - | 6.09 | ZNF263 | MA0528.1 | chr1:212403026-212403047 | TTTTCCCTCCTCCCTTCCTCT | - | 6.13 | ZNF263 | MA0528.1 | chr1:212401156-212401177 | GAAGAAGGAAGAAAAAGGAGA | + | 6.46 | ZNF263 | MA0528.1 | chr1:212402664-212402685 | CTTTCCTTACCTTCCTCCTTT | - | 6.57 | ZNF263 | MA0528.1 | chr1:212403018-212403039 | TTTCTTTCTTTTCCCTCCTCC | - | 6.7 | ZNF263 | MA0528.1 | chr1:212401350-212401371 | CCCTCTTTCCCATCCTCCTTA | - | 6.88 | ZNF263 | MA0528.1 | chr1:212403029-212403050 | TCCCTCCTCCCTTCCTCTCCC | - | 6 | ZNF263 | MA0528.1 | chr1:212401347-212401368 | TTTCCCTCTTTCCCATCCTCC | - | 7.01 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_00506 | chr1:212397824-212401716 | Adipose_Nuclei | SE_31662 | chr1:212400859-212401451 | Gastric | SE_31662 | chr1:212401468-212402631 | Gastric | SE_31662 | chr1:212402726-212404120 | Gastric |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr1 | 212403042 | 212403200 | chr1 | 212403200 | 212403432 | chr1 | 212401476 | 212401801 | chr1 | 212401929 | 212402431 | chr1 | 212403027 | 212403223 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I212227 | chr1 | 212400860 | 212401451 | GH01I212228 | chr1 | 212401481 | 212403276 |
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Enhancer Sequence | GGTTCCCAAT TCCCAAATCA TATAACATTT TCCAAAATGT TTCCCAATAT GTCTTCTAAC 60 AGATGTTTGT GTGTGTGTGT GTTTTAAAAA ATTTCAGTAG CTTTTGGGGT ACAAATGTTT 120 TTGGTTACGT GGATGAACCG CAGAGTGGTG ACGTCTGACA TTTTCATGCA CCCATCACCC 180 AAGTAGTGTA CATTGTACCC AATATGTAGT TTTTTATCCC ATACCCCTCT CTCATCCTCC 240 CTCTTCTGAT TCTCCAAAGT CAATGGACTT TGGATGTTTT TTTTTCAAAC AAGATCCAAT 300 CAAAACTCTT ACATTGCATT TGGTTGTCAT GTCTCTATTT TCTTTTATTC TAGAGCGGTA 360 GGTGTGGGGA AATTTTGAGA ACAATATTGT TGCTGAAATC AACTATTGGC TGCCAGGTGG 420 AAATGGCTGC TGCCTCCACT GAGGCACACT GGGCCCCGCC ACATTTATTA GCACAAGCCC 480 TGTGATATGG TTGCATAGCT TGCTTTGCTG AACTTGTTGG TTACTAGCTA CTGCTTAATG 540 ACTGGACATT AGAGACTCTT CTGTTGTTTT TATATTCCCA CCACCTCCAC AGCACCTAAC 600 ACACAGGTGG TCAGTAAAAG TGGATGGAAG GAAAGGAGGC AGGGAGGAAG AAGGAAGAAA 660 AAGGAGAGTG GGAAAGAGGC AGGCACGGGC AGGCCCCCCT GCCTCCATGC CAGGTGGGTA 720 CCTGGAGAGT GACACTGTGC CCTCCTGGGA AGCACCCACA CTCCTTTGAT TGGGGGAAAA 780 CGATTCCATG TGGCATGTGC CTTTTGTCCA AATATGCCTT CTTCCTTCGC ATTCTCCTTT 840 CCCTCTTTCC CATCCTCCTT ACCTGAGCAC TAGTTGGGAT CCCTCAGACC TTCTGCTATC 900 TTTAACTTAG TCTTTCCCTC TCTTCCCATA TACAAGATTA ACATTTGACA TTATTTTAAA 960 AATAATCTGT AATAGATTAT CTTTTCCTAC AATCACACTC ATTTTCCCAA TTCCCTGGGA 1020 GATAATTCCC ACAAAATTTG TGGTCAGTAA TTAAATTCCT GACCACAATG AATCATGAGG 1080 AATATATACT GTGTTCAGAG GGATGGCGTG GTATCCGTAA GGGAGCATCT GCTGAAGGGA 1140 GAGAGAGGAC ACATGGGGGT TAGCCCACAA AGCCAAGGGG AGCTGTCCTC CAAACACAAC 1200 CAACAGAGTT TAGCTCAGGC TTCAGGATCA AACTATTGCT TCTATTCTGT GTGGAGAGAA 1260 CAATGACTGA ATTGGCTGGA ATAGAACAAA GTTGTTAAAG TGAACTTTCT CCACACCTCA 1320 TCTCTAATCC CTAAAATTTT GACTTAAACA AAATTTTGAG TTAAGCAAAT TTGAATTAAA 1380 AATTTTGAGC AGATACAGGG AATGAATGCA AGAAGCTCTT GATTATCTTC ATGGTGGACT 1440 GGCTCATTTT CATTCCGGGC TGACCTCGTT GATATGTTCT CTACCACTTC TCCTTGCTGA 1500 GAAGTAGTTG GCGTCTATTC AAAGTACACA GGCCATTTAA TTATTAATCG GAGCAAAACA 1560 TTATTAGGGA AGTTAAACTG TTGAGTAGGT GTGTGTGTGT AAACATGTGG ATACTTTCTT 1620 GATTATCTAG CTGTTTTGTT TTGCCTTTTG CCTTTCTGGG TTCCTGCCCC TCTCCATTTG 1680 TGGTGATACC TGTAAGGTGA TTATGCCACT GAATTCCTAA GAGCTTTTTG GTCCCTCTCT 1740 CATTCTCCTT GGATGTGTGT GGAAATGTTT GTCAGCAGGG GCGGACCGGG GAGGGTTCAT 1800 GTACACAAGA AGTGACTGAC CTTGGCCGCT GAGTGGAGTG TGTATTTGTG ACGAGGAAAG 1860 GGTTCAGTGT TTGTGTTTGG TGATGGTTTT ATGTCCTGCT GTCATTAGAG AGGACTTTAT 1920 AGGGGTTTCT GATGACCTAG GGCTCCAGGA ATCATCATGA TTATTTAGAC AATGATTTTA 1980 ATGGGCCCAT ATAAACTTAT TCTGTTTTTA TACTAGTAAC AGAGAAGAAG ATGTTGGAAG 2040 ATTAAATATA GAGAAGGATG GGCTTTAGCG TCACTGTTCA GGGACATTGG GAATTATTCT 2100 ACAGAATTCG ATCCAGCCTA TTCTCATTAT TTCCTTCTTC TTATGACTTT CATTCTTTCC 2160 TTACCTTCCT CCTTTTCCCT TTCTTCTTCT TCTTTTTTTT TTTTTTGAAA CGGAGTCTCT 2220 CTCTGCCGCC CAGGCTGGAG TGCAGTGGTG CAATCTCAGC TCACTGCAAG CTCTGCCTCC 2280 CAGGTTCACG GCATTCTCCT GCCTCAGCCT CCCAACTGGC TGGGACTACA GGCGCCCGCC 2340 ACCATGTCCA GCTATTTTTT TGTATTTTTA GTAGAGACAG GGTTTCACTG CCTTAGCCAG 2400 GATGGTCTCG ATCTCCTGAC CTTGTGATCC ACCTATCTCG GCCTCCCAAA GTGCTGGGAT 2460 TACAGGCGTG AGCCACTGCG CCCGCCCTCT TCTTTTTTTC TTCCTTGCTT TCTTTCTTTT 2520 CCCTCCTCCC TTCCTCTCCC CACCTTTATT TATTTCTTTC AACATGTACT GCCTGCTTAC 2580 TATATATTAG TCACAGTCTA AATGCTGGAG ATGCAGAGAT GAATAACACA TGGCCCCAGC 2640 CCTCCTGGAA CTCAGTTTAG CGTGGGAGGC AGATGGAGGC ACAGATCATT CCAGTACAGT 2700 GGTTAACGAT AGAGATAAGT ACAGGGTGAG CTCAATGTAG GGGTCCCTAA TCCAGCTTGG 2760 CTTGGGAGAG AAGGCAGGAA GCTTCCTGGA AGAGATGATG GCAGATTGAT TGGGAGTGGC 2820 TGAAAAAGGA GCAGGGCTCA AGGCCTTTAC CTGGCAGGCC AGGTCATTCA CATGGTTTAT 2880 GAGCACTGGA TAAAGGGAAT GGGATGAAGG GCTTTGGGGG TATGGGTCTT CCATGAGATA 2940 TGACACCAGA TTTTGATGTC ACTGCATATG GTTAGGACCA CAGGGGCAGG GCAGAAATGA 3000 TGTCTACTAC TGTGGGACAG TACTAGTGAC 3030
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