Tag | Content |
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EnhancerAtlas ID | HS082-20671 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr2:237779000-237781300 |
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) |
CDX2 | MA0465.1 | chr2:237781195-237781206 | TTTTATGGCTC | - | 6.14 | NFE2L1 | MA0089.2 | chr2:237779089-237779104 | ACTGCTGAGTCACTA | - | 6.52 | Nfe2l2 | MA0150.2 | chr2:237779091-237779106 | TGCTGAGTCACTACT | - | 6.04 | SOX10 | MA0442.2 | chr2:237781215-237781226 | AAAACAAAGCA | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 237779025 | 237779410 | chr2 | 237779904 | 237781044 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I236870 | chr2 | 237778967 | 237781662 |
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Enhancer Sequence | GTAACTTATC TGGTCCTGAG GTCCCATTCG AGTCTCCTCA ACATTGCAAA GTCTTTCCCA 60 AGCTCACCTT CTCACTGTCC CCTGCCCTCA CTGCTGAGTC ACTACTTTGC CTTATAGGGT 120 CCCTGTAGTT GAACAGTGAT TTACTGATTA GACTGCACAG TAAAATGGAT GGTTGCGTTT 180 ATTCCTAAGC AGTTGATTTT TTCTCACTTT GCACAGGAAG AACCAAAGCG CAGTAAAAAA 240 AACAGTGTCT TGTTCAAGCC CACACAGCTG ATAAGATTAT GTTCAAGCCC ACACAGCTGA 300 TAAGATTAGG CAGAACCAGA ACCCACACCT TCGTGTGAAT CTAGGCTCCT TCCAGCAGGC 360 CACACATGGC CTTGGGCTAT CATTTGAGTG TATATTTCAC AGGGGTATTT CTTGATGCCA 420 TTTATGGTGG CACTACTTTT TATACCTTTG AAGTCCTCCC AGAGCCTAGT TGAGTGCTGG 480 GGATACTTAG GCAAGTGTTA CTGAGTGACT GAGGGAAGGT GTAAGAAGAA GGTAGTAATC 540 ACTATAAGGA CATGATAGTC TTGCTAAGCA AGACAGGCAC TGAAGGAAGA CTCCCAATGT 600 TGGAGGTGTC AAGGAAGGTA ACACGGAGCC TCCCCAGCTT CCACCATAAG AAAGGTTGTC 660 AAAAAGATTT TCTTGGGATT CTTAAGCCTC TCTGTTTAAA TATACAAAAA GTTCGAGCTT 720 TGGCTATTAA CAATTAATGT CTAAAGTACA ACCTAAGTAC CAGAAATATA AATACATTTT 780 TCAATATATG TCCCCTAAAG AATGAGGAAC CAATAATTTA TAATTGTCCA ACAACATTCT 840 TTTCTCCAAA TGGAAAAGCC CCAAGTCCTT TACTTATTCA ATGAGGAAAA ACACAGTTAC 900 CCCATTTGTC TTGTTTTCTA AACATTTGAC CATTTTCTTA GCCTCTCTGT GAACTGGCTT 960 TTTGATAGCA CCCTTCAATT TTGGAGACTC ATCTGGAGAT GGTTTTATAA TGGTGGCCCA 1020 GTTGATGCCA AGTATCTCTT AAAATGGTCT TCTTGTAAAC ATGTGGTGAC ACTTTATTAC 1080 CTCTTTCCAT AACATGATTC CATTATGAAC ACATACTTTA TTACTGGTCA GGAACTAGCT 1140 CTACATCATT CTCAAGGATG GGTGTATGTG AGCTCTCTTC TCTTGACCTA TATTTACTAT 1200 TCTAGTGATT CATACTCTGT GTATATCCCT ATTGCATTAC TTCCTGTTTG CAACAGAGCA 1260 ACCACAGAAC AGTCTGGACA AAGCCATTTC CTTCTTCTTT TAATACTTAT TTACGTGTTG 1320 CTCCAGTGAG TATGTGCGCA GGGTTGCTGT GCAAAGTGTG GTGAGCCTGG TGTCCTCAGG 1380 AAACTAACAC CAGCTGTCAA GAGGGCTTAG GAAAATACCC TGGAGCTGGC GTCAGCCACA 1440 GAATCGAGTG AGGAAAAGGG GAGCAGGCCT GACTATTTCA CTGACTCATC CTGTCTCCTT 1500 TTCCAAGTCA CTTCCTGTCA AAGCGGGAAC TTCCCATTAG TTCCACATAA GTAGAGCTCT 1560 TCCAGACATG TACAGGGTGA GATCAGCAAT ACACTTCTTT CCTTTAGTAG CTTTCAAGTT 1620 ACTATCATCG TAAGCTGGCA AATTTAATAT TGCGTGTCTT GGATGGTGGG AGCAAAAAAG 1680 CCTATTTAAC CTGAACAGAA CCCACACTTG TCCATGTTAT GCTTTATCTA TTTGTTCATT 1740 CATTCATTCT GTCAACACAC TTACGGTAAA CTCCTGTGTG TAACATGTTA CGCTTGTGTC 1800 TAGGTCTGCA AATAACCCCA TGTTTAGAAG TTCATGGTCA GCAGGTTCCT CAGCAAACTC 1860 TGCCAGTGCC GCCCACTGAC CCAAGCAGAG GAAGCAGATG CATCTTGAAC AGATTTTCAC 1920 ATGGAATGTA GTATCTCTCC TCATGCTGTC TGGACAGGAA TACAGGTTAA CTCTAGGAAA 1980 GCTGCAAGTT ACAGCAGATT GAGCGTGAAC TTAGGAGCCA GCAGGTCAAG CCATGGCACT 2040 CAGTAGTTGG ATAAACTTGG GCACATTACC TAACCTTCTG AACTGTAAAA TGGAGCTAAA 2100 GATAAAACTC CTTCCAAAGA GTTGTTATGA CAATTAAATG CAATGTTTTA TATGAAGTCC 2160 TTAGTACAAC TACATGCAGG AAGGATTTGC TCGAGTTTTA TGGCTCTTAT TATTGAAAAC 2220 AAAGCATATC AAAAACAAAA CCCTTTACCT ATTTAATCTG GAGTCAATAT TCTGCACAAA 2280 ATGACACTTT TATAATTAGT 2300
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