| Tag | Content |
|---|
EnhancerAtlas ID | HS102-00588 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr1:29574940-29577010 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 | GGGTTGTATT TGAATTCCCC CACCCACAAC TGGGCATGTA CCTGGGCTTG GGTGAAATCC 60
CAGCCCCTAA ATGTGCAACC TGTTGGGAAA AGTTTTGCTT CTCCTGGGAC CACTCTTGGG 120
AATTGGATGT TCTATTGACA AACCAAAGGG CAGAAAAGTC TCATTGCAAA CAGGCTCTGT 180
TTGCCAGGTG TCTTCAGAAA ATACTGGTTG CAGCTGCAGC CGCATTGGGC ATGGAGTGCT 240
GTTCCCTGTC TGGTGTGAGG AAAGTCTGGT GCACAGTGCT TGTGTTCACA CTGACACATA 300
CACGTATGCA CAACTCCCAT CTACCTTACT GCACACACCC ACCTCCCCCT TAGGTGCAGG 360
CTTACCACTA AATATGCCCT GTACCTTTGC TTGTAAATGC ACGTCTATAC ACCCACGGCT 420
TCACAGCGCC TGCCCGGGAG ACCTCCCCTT TCCGACACCC ATGCCCACCC TCATGCACCT 480
CTGCCCCAAG ATGACTCTTG CTCACGTGCA CACTCACGCA ACTGCAACCG GTCATCTGAC 540
CTTAGCGGTC CCCACTCTCA TTTTACAGGT GAGGAGGTAA GGATTCAGAG AGGGCAAGTC 600
ACCTGCCCAA AGTCACAAAG GGACTTAGAG GCTCAGTGGG AAAAAGATCC CGGTCTTCCG 660
CCTCCCATTT GAATACTTGA AACTCAGTAC CAGGCTGTCC TGTCATCTTA GAGCCATGAG 720
TGCACGTGTG CACACACACA CACGCACACC TGCACACACT CACACGCACA CCTGCATGTG 780
GACACATGCA TGGGGAGGTG TGGAGCCCCT CCCACCAGGG AGACCCCTCC CACACTCCTC 840
CAGAGGCAGC TCTGCCCCTT ACATCACCCC ATCCTGAGCC CAGCCGGATG TGGCTAAACC 900
ATCCCCCTGC CTTCCCAAAT TGTGGCTGAC GGTTGCTCAG GCAACCGCCT GCCAGACTGG 960
GGAGATTAGC TGAGGAATGT AGCTGGGCCA GTTTGAACTG AGGCTGGGGG AGCCCTTGGG 1020
GGTCTTGGGT TGATTCAATT CACCCTCTCA GGGAGGCCTC TGTAGAGATG GGGTGCCCAA 1080
GGGCAGGCAT TCTCCCTGTT CCCAGTCTGA GGCTGCATCC CCAGGCTTGG CCCAGGCTGC 1140
AGAAAGGGAG TGTGTGTGAA CACTGAGCGC GGGGCTCAGG GCATATGTGT GTTGTGTGCT 1200
GTGCACCTCT CTGAGTGTGA TTGGAGGGTG TGCCGTTTAC ATCCTGGAAG GGGACTTGAG 1260
GCCCCTGTCC TCACCAGTTT CTGACATCTG ACTCTGGACC CCTTGGTGGC TTGGTCCCAA 1320
GATCCCTCTG GATCCTGCTG TGCTCTCTGG AGACACCACC TGCCCTACTC ATGGCTTATA 1380
GGATATATCA TTTATCTCAT CTGAATCCAG GATGAGATAA ACTTTCCTAC TCAAACACCT 1440
ACTGTGGCTT CTCAATTCAA AATGAGGCCC AGCTCCTCAC CCTGGCGTTC AGGGTCCTCC 1500
ATGATTGGCC TCAACCTCCC TTCCCTCCAG TCATAGCTCC CATGGCTTTA GCCAACCTGG 1560
GCTCCTTTCT GTGCCCTGGA CAAACTGTGT TTATTGACCA CCTTGCTTTG CTCCCCTGGG 1620
TCTTTTGCCA CAAATCCTTC CACCCATCTC TACCTATCCT TCTTGGCTCT GCTTAGATGC 1680
CGCCTCTTCC AGGAGGCCTT TCCCCTCTAC CTGGCCCCCT CCCCTGGACC CCCTCTTGTG 1740
GCCTTGACTC TTCCCTTATT CCCTCATTCC CTCTTCCTCA CCCTCACTGG GACTAGGAGG 1800
TCCCTGAGGG CAGGGCAGAG TCTTCATCAT CCTTGTACCT CTAATAGTGC CAGCCTGGGA 1860
CCTGCTTTGT ACTGGCAGGG AAAAATCCCC TGTGAATGAA GCTGAATTAA CACTTATGGC 1920
CAGCAGAAGG GCAGGCTTTG TTTTGTTTGT GCCCAGTCTC CTGGAATAAA GATAGGAGGT 1980
TTAAGTCTGA GCTTCTGCAC ATTGTAGCTG CATGGCCTTG AGTAAGCAGC TGTATCTCTC 2040
TGAGCCTGTT TTAATCTGTA AATTAGGAAT 2070
|
