Tag | Content |
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EnhancerAtlas ID | HS118-10064 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:73912700-73914280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:73912902-73912920 | CATGCCCTCCCTCCTTCC | - | 6.37 | NFYB | MA0502.1 | chr2:73912861-73912876 | CTGATTGGTCCAAGT | - | 6.77 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 73913200 | 73913580 | chr2 | 73912886 | 73912957 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I073685 | chr2 | 73912747 | 73913897 |
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Enhancer Sequence | AAATTCTAAT TTAACCAGTA AGCAATATGT AAAAGGAAAT CTGAATGTCA TTACAATTTT 60 ACCAGGTTCA GAATAAAATA CCATCCTTCA AAATGAACAA ATTACTTATT AGCCGAAGAA 120 AGGTGAAAGG AAGTTTGGAA TTAACAGTCT AGATTTTCTC ACTGATTGGT CCAAGTCACT 180 GACCTCTAAA ATTATCTTAG ATCATGCCCT CCCTCCTTCC TACTTTCTGG AAAACAATCA 240 GTCTCCTACC CTATGCTTGC CCAAAGAGTT TCCCATACAA ATCACAAATC TGCACTTGCC 300 ATTCCCTGGA AGCCCTTACA TTCCCAAGGC CTGGCCTCAT CCACTGCCAC TGCCCATGGC 360 CCCAGTCCAG GCAAAGCAAT CACTCCCTCT CCCTCTCTGT CATTCCTTTC TTTTCCTTTC 420 ACTCTCTTTC TACCCTCCTC TTCCCCACTC TCTGTTTCCT CTCTCTCTCT CTATCTCTCT 480 CTCCCCACCA TCTCCTCTCT CTGTCTCCCC CCGCCTTCTC TCTCTGTCTC TGTCTCTCTG 540 TTTCTCTGTG TCTCTCTCTC TGTCTCTCTC TTTGTCTCTC TCTCTGTCTC TCTCTCACAC 600 ACACACACAC ACACACACAC GCACACACAC ACACAGCCAG CAACATTCTA CCTCTGCCAG 660 AGTTCCAGGT TGAATAGGTG TGGACTTTGA CTTTCAGATT CCTCTGGCAA GTGTCAACAT 720 CAGTCCTGTT GCTCCCTGGC AGAGGAGGAC TTGGAGTCAC CTTGGCCAAG AAGCTGTCTG 780 GAGGTCACAG TGGCACCGCC CATCGGCCCC TTGGCTGAGG CTAGATGAGG GCAGATTCAG 840 CACAGCAGCA ACTCTCCCCA TAAAAAAAAT CCCTCAGTGT CTTAGTTCTC TGACCCTTGT 900 ACTCCTTGTG AGTTTTAGAG CCACATGAAC TCTTCTTTTT TCCCAATGCT TGGAGACAAA 960 ATTTACATAA CCTACAGTTA GCCATTTTCA AGTGTACAGT TCCCTGCCAT TTGGTACATT 1020 CACAGTGTTT TGCAAGCAAC ACCCATATCA AGCCCCAAAA CATTTTCATT ACCCAGGAAG 1080 GAAACCTGTC GTCATGGAAC CGTCACTCCT CACATCCCCT TCCCCTCAAA CCCTGGCAAC 1140 CCCAAACCGT TCTTGACAGC CTCCTTTGGC ATTTCTTCAT TTTGGTGTCA GATCTCACAG 1200 CAGAATTTCT TACCTATTAT ATCCAGTGCC TCAGTGCGAA GTTCCAGTTT AACTTCCTGT 1260 TACCTCGAGC CCACTATCTT GCCCCAATAA TACCCTCCCC CAATTCACAA ACACAGACGC 1320 ATTCCCTCCT ACAGCTTTGG GCCTCCTATC TGAGTCCTTC AGGAAAGAAG AGCTTGTAAC 1380 TCCCTTAGCA GTGAGTGTAG ACTTGGTCCA AGGAAGATGA GCACCAGTCA GGGCAGCTGG 1440 CCCCTCCTCT CTCCCTGGTC TTCAGCAAAT CAGCACTGCC CATCGATGCC CAGGCAATGG 1500 GAGCGTCGAC CAGCAGAGGA CACACCTGAA TTTCTCTGCC TCATGGGAGG GCGGCCACTG 1560 TGTTGCATTT AGGAAGAAGC 1580
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