Tag | Content |
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EnhancerAtlas ID | HS041-00829 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chr1:29575170-29576650 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SREBF2 | MA0596.1 | chr1:29575802-29575812 | ATCACCCCAT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I029247 | chr1 | 29574480 | 29577515 |
| Enhancer Sequence | ATGGAGTGCT GTTCCCTGTC TGGTGTGAGG AAAGTCTGGT GCACAGTGCT TGTGTTCACA 60 CTGACACATA CACGTATGCA CAACTCCCAT CTACCTTACT GCACACACCC ACCTCCCCCT 120 TAGGTGCAGG CTTACCACTA AATATGCCCT GTACCTTTGC TTGTAAATGC ACGTCTATAC 180 ACCCACGGCT TCACAGCGCC TGCCCGGGAG ACCTCCCCTT TCCGACACCC ATGCCCACCC 240 TCATGCACCT CTGCCCCAAG ATGACTCTTG CTCACGTGCA CACTCACGCA ACTGCAACCG 300 GTCATCTGAC CTTAGCGGTC CCCACTCTCA TTTTACAGGT GAGGAGGTAA GGATTCAGAG 360 AGGGCAAGTC ACCTGCCCAA AGTCACAAAG GGACTTAGAG GCTCAGTGGG AAAAAGATCC 420 CGGTCTTCCG CCTCCCATTT GAATACTTGA AACTCAGTAC CAGGCTGTCC TGTCATCTTA 480 GAGCCATGAG TGCACGTGTG CACACACACA CACGCACACC TGCACACACT CACACGCACA 540 CCTGCATGTG GACACATGCA TGGGGAGGTG TGGAGCCCCT CCCACCAGGG AGACCCCTCC 600 CACACTCCTC CAGAGGCAGC TCTGCCCCTT ACATCACCCC ATCCTGAGCC CAGCCGGATG 660 TGGCTAAACC ATCCCCCTGC CTTCCCAAAT TGTGGCTGAC GGTTGCTCAG GCAACCGCCT 720 GCCAGACTGG GGAGATTAGC TGAGGAATGT AGCTGGGCCA GTTTGAACTG AGGCTGGGGG 780 AGCCCTTGGG GGTCTTGGGT TGATTCAATT CACCCTCTCA GGGAGGCCTC TGTAGAGATG 840 GGGTGCCCAA GGGCAGGCAT TCTCCCTGTT CCCAGTCTGA GGCTGCATCC CCAGGCTTGG 900 CCCAGGCTGC AGAAAGGGAG TGTGTGTGAA CACTGAGCGC GGGGCTCAGG GCATATGTGT 960 GTTGTGTGCT GTGCACCTCT CTGAGTGTGA TTGGAGGGTG TGCCGTTTAC ATCCTGGAAG 1020 GGGACTTGAG GCCCCTGTCC TCACCAGTTT CTGACATCTG ACTCTGGACC CCTTGGTGGC 1080 TTGGTCCCAA GATCCCTCTG GATCCTGCTG TGCTCTCTGG AGACACCACC TGCCCTACTC 1140 ATGGCTTATA GGATATATCA TTTATCTCAT CTGAATCCAG GATGAGATAA ACTTTCCTAC 1200 TCAAACACCT ACTGTGGCTT CTCAATTCAA AATGAGGCCC AGCTCCTCAC CCTGGCGTTC 1260 AGGGTCCTCC ATGATTGGCC TCAACCTCCC TTCCCTCCAG TCATAGCTCC CATGGCTTTA 1320 GCCAACCTGG GCTCCTTTCT GTGCCCTGGA CAAACTGTGT TTATTGACCA CCTTGCTTTG 1380 CTCCCCTGGG TCTTTTGCCA CAAATCCTTC CACCCATCTC TACCTATCCT TCTTGGCTCT 1440 GCTTAGATGC CGCCTCTTCC AGGAGGCCTT TCCCCTCTAC 1480
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