Tag | Content |
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EnhancerAtlas ID | HS037-00574 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr1:29575200-29577400 |
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) |
SREBF2 | MA0596.1 | chr1:29575802-29575812 | ATCACCCCAT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I029247 | chr1 | 29574480 | 29577515 |
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Enhancer Sequence | AAAGTCTGGT GCACAGTGCT TGTGTTCACA CTGACACATA CACGTATGCA CAACTCCCAT 60 CTACCTTACT GCACACACCC ACCTCCCCCT TAGGTGCAGG CTTACCACTA AATATGCCCT 120 GTACCTTTGC TTGTAAATGC ACGTCTATAC ACCCACGGCT TCACAGCGCC TGCCCGGGAG 180 ACCTCCCCTT TCCGACACCC ATGCCCACCC TCATGCACCT CTGCCCCAAG ATGACTCTTG 240 CTCACGTGCA CACTCACGCA ACTGCAACCG GTCATCTGAC CTTAGCGGTC CCCACTCTCA 300 TTTTACAGGT GAGGAGGTAA GGATTCAGAG AGGGCAAGTC ACCTGCCCAA AGTCACAAAG 360 GGACTTAGAG GCTCAGTGGG AAAAAGATCC CGGTCTTCCG CCTCCCATTT GAATACTTGA 420 AACTCAGTAC CAGGCTGTCC TGTCATCTTA GAGCCATGAG TGCACGTGTG CACACACACA 480 CACGCACACC TGCACACACT CACACGCACA CCTGCATGTG GACACATGCA TGGGGAGGTG 540 TGGAGCCCCT CCCACCAGGG AGACCCCTCC CACACTCCTC CAGAGGCAGC TCTGCCCCTT 600 ACATCACCCC ATCCTGAGCC CAGCCGGATG TGGCTAAACC ATCCCCCTGC CTTCCCAAAT 660 TGTGGCTGAC GGTTGCTCAG GCAACCGCCT GCCAGACTGG GGAGATTAGC TGAGGAATGT 720 AGCTGGGCCA GTTTGAACTG AGGCTGGGGG AGCCCTTGGG GGTCTTGGGT TGATTCAATT 780 CACCCTCTCA GGGAGGCCTC TGTAGAGATG GGGTGCCCAA GGGCAGGCAT TCTCCCTGTT 840 CCCAGTCTGA GGCTGCATCC CCAGGCTTGG CCCAGGCTGC AGAAAGGGAG TGTGTGTGAA 900 CACTGAGCGC GGGGCTCAGG GCATATGTGT GTTGTGTGCT GTGCACCTCT CTGAGTGTGA 960 TTGGAGGGTG TGCCGTTTAC ATCCTGGAAG GGGACTTGAG GCCCCTGTCC TCACCAGTTT 1020 CTGACATCTG ACTCTGGACC CCTTGGTGGC TTGGTCCCAA GATCCCTCTG GATCCTGCTG 1080 TGCTCTCTGG AGACACCACC TGCCCTACTC ATGGCTTATA GGATATATCA TTTATCTCAT 1140 CTGAATCCAG GATGAGATAA ACTTTCCTAC TCAAACACCT ACTGTGGCTT CTCAATTCAA 1200 AATGAGGCCC AGCTCCTCAC CCTGGCGTTC AGGGTCCTCC ATGATTGGCC TCAACCTCCC 1260 TTCCCTCCAG TCATAGCTCC CATGGCTTTA GCCAACCTGG GCTCCTTTCT GTGCCCTGGA 1320 CAAACTGTGT TTATTGACCA CCTTGCTTTG CTCCCCTGGG TCTTTTGCCA CAAATCCTTC 1380 CACCCATCTC TACCTATCCT TCTTGGCTCT GCTTAGATGC CGCCTCTTCC AGGAGGCCTT 1440 TCCCCTCTAC CTGGCCCCCT CCCCTGGACC CCCTCTTGTG GCCTTGACTC TTCCCTTATT 1500 CCCTCATTCC CTCTTCCTCA CCCTCACTGG GACTAGGAGG TCCCTGAGGG CAGGGCAGAG 1560 TCTTCATCAT CCTTGTACCT CTAATAGTGC CAGCCTGGGA CCTGCTTTGT ACTGGCAGGG 1620 AAAAATCCCC TGTGAATGAA GCTGAATTAA CACTTATGGC CAGCAGAAGG GCAGGCTTTG 1680 TTTTGTTTGT GCCCAGTCTC CTGGAATAAA GATAGGAGGT TTAAGTCTGA GCTTCTGCAC 1740 ATTGTAGCTG CATGGCCTTG AGTAAGCAGC TGTATCTCTC TGAGCCTGTT TTAATCTGTA 1800 AATTAGGAAT AATAATAGTA CCTAATAAAC TAACAATAAG ACAAAAATAA TACTACCTAC 1860 CTTCTGAGTT GCTGAGGATT CACCGGCTCA GGTGGTCATG GTGGTAATTC ACAGCCCCTT 1920 CATAGAGGTA TTGATGTGTA TATGTGCATG TCTGTGCCCA TGTCTGTGTT GATGGAGTCA 1980 AGAAGGATTC CTTGCTACCA TTCTTGCTCT GAACTCAAAG TCGGATTTAG TGGCCTCCAG 2040 CAGGAGTTGA GTCTCTAGCA GAGCTGGGAC TTGGCTTTGG GGCTTTTGGC TCCTAGCTGA 2100 CCATTCCCAT CTCAAGGGAC CAGGGGAAGG GGTGAGGGTG GGGCTCTCCT TAGGGAGCCT 2160 GTCCCCAGAG ATGTTACCCA CTATGAGCTG GAGCTAGAAC 2200
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