Tag | Content |
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EnhancerAtlas ID | HS095-00671 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:29575130-29576800 |
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 | TCTTCAGAAA ATACTGGTTG CAGCTGCAGC CGCATTGGGC ATGGAGTGCT GTTCCCTGTC 60 TGGTGTGAGG AAAGTCTGGT GCACAGTGCT TGTGTTCACA CTGACACATA CACGTATGCA 120 CAACTCCCAT CTACCTTACT GCACACACCC ACCTCCCCCT TAGGTGCAGG CTTACCACTA 180 AATATGCCCT GTACCTTTGC TTGTAAATGC ACGTCTATAC ACCCACGGCT TCACAGCGCC 240 TGCCCGGGAG ACCTCCCCTT TCCGACACCC ATGCCCACCC TCATGCACCT CTGCCCCAAG 300 ATGACTCTTG CTCACGTGCA CACTCACGCA ACTGCAACCG GTCATCTGAC CTTAGCGGTC 360 CCCACTCTCA TTTTACAGGT GAGGAGGTAA GGATTCAGAG AGGGCAAGTC ACCTGCCCAA 420 AGTCACAAAG GGACTTAGAG GCTCAGTGGG AAAAAGATCC CGGTCTTCCG CCTCCCATTT 480 GAATACTTGA AACTCAGTAC CAGGCTGTCC TGTCATCTTA GAGCCATGAG TGCACGTGTG 540 CACACACACA CACGCACACC TGCACACACT CACACGCACA CCTGCATGTG GACACATGCA 600 TGGGGAGGTG TGGAGCCCCT CCCACCAGGG AGACCCCTCC CACACTCCTC CAGAGGCAGC 660 TCTGCCCCTT ACATCACCCC ATCCTGAGCC CAGCCGGATG TGGCTAAACC ATCCCCCTGC 720 CTTCCCAAAT TGTGGCTGAC GGTTGCTCAG GCAACCGCCT GCCAGACTGG GGAGATTAGC 780 TGAGGAATGT AGCTGGGCCA GTTTGAACTG AGGCTGGGGG AGCCCTTGGG GGTCTTGGGT 840 TGATTCAATT CACCCTCTCA GGGAGGCCTC TGTAGAGATG GGGTGCCCAA GGGCAGGCAT 900 TCTCCCTGTT CCCAGTCTGA GGCTGCATCC CCAGGCTTGG CCCAGGCTGC AGAAAGGGAG 960 TGTGTGTGAA CACTGAGCGC GGGGCTCAGG GCATATGTGT GTTGTGTGCT GTGCACCTCT 1020 CTGAGTGTGA TTGGAGGGTG TGCCGTTTAC ATCCTGGAAG GGGACTTGAG GCCCCTGTCC 1080 TCACCAGTTT CTGACATCTG ACTCTGGACC CCTTGGTGGC TTGGTCCCAA GATCCCTCTG 1140 GATCCTGCTG TGCTCTCTGG AGACACCACC TGCCCTACTC ATGGCTTATA GGATATATCA 1200 TTTATCTCAT CTGAATCCAG GATGAGATAA ACTTTCCTAC TCAAACACCT ACTGTGGCTT 1260 CTCAATTCAA AATGAGGCCC AGCTCCTCAC CCTGGCGTTC AGGGTCCTCC ATGATTGGCC 1320 TCAACCTCCC TTCCCTCCAG TCATAGCTCC CATGGCTTTA GCCAACCTGG GCTCCTTTCT 1380 GTGCCCTGGA CAAACTGTGT TTATTGACCA CCTTGCTTTG CTCCCCTGGG TCTTTTGCCA 1440 CAAATCCTTC CACCCATCTC TACCTATCCT TCTTGGCTCT GCTTAGATGC CGCCTCTTCC 1500 AGGAGGCCTT TCCCCTCTAC CTGGCCCCCT CCCCTGGACC CCCTCTTGTG GCCTTGACTC 1560 TTCCCTTATT CCCTCATTCC CTCTTCCTCA CCCTCACTGG GACTAGGAGG TCCCTGAGGG 1620 CAGGGCAGAG TCTTCATCAT CCTTGTACCT CTAATAGTGC CAGCCTGGGA 1670
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