| Tag | Content |
|---|
EnhancerAtlas ID | HS080-00687 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:29574900-29576980 |
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 | GTACAACCTT GGATGATGAA ATAGTCCAGT ATTGTTGTTG GGGTTGTATT TGAATTCCCC 60
CACCCACAAC TGGGCATGTA CCTGGGCTTG GGTGAAATCC CAGCCCCTAA ATGTGCAACC 120
TGTTGGGAAA AGTTTTGCTT CTCCTGGGAC CACTCTTGGG AATTGGATGT TCTATTGACA 180
AACCAAAGGG CAGAAAAGTC TCATTGCAAA CAGGCTCTGT TTGCCAGGTG TCTTCAGAAA 240
ATACTGGTTG CAGCTGCAGC CGCATTGGGC ATGGAGTGCT GTTCCCTGTC TGGTGTGAGG 300
AAAGTCTGGT GCACAGTGCT TGTGTTCACA CTGACACATA CACGTATGCA CAACTCCCAT 360
CTACCTTACT GCACACACCC ACCTCCCCCT TAGGTGCAGG CTTACCACTA AATATGCCCT 420
GTACCTTTGC TTGTAAATGC ACGTCTATAC ACCCACGGCT TCACAGCGCC TGCCCGGGAG 480
ACCTCCCCTT TCCGACACCC ATGCCCACCC TCATGCACCT CTGCCCCAAG ATGACTCTTG 540
CTCACGTGCA CACTCACGCA ACTGCAACCG GTCATCTGAC CTTAGCGGTC CCCACTCTCA 600
TTTTACAGGT GAGGAGGTAA GGATTCAGAG AGGGCAAGTC ACCTGCCCAA AGTCACAAAG 660
GGACTTAGAG GCTCAGTGGG AAAAAGATCC CGGTCTTCCG CCTCCCATTT GAATACTTGA 720
AACTCAGTAC CAGGCTGTCC TGTCATCTTA GAGCCATGAG TGCACGTGTG CACACACACA 780
CACGCACACC TGCACACACT CACACGCACA CCTGCATGTG GACACATGCA TGGGGAGGTG 840
TGGAGCCCCT CCCACCAGGG AGACCCCTCC CACACTCCTC CAGAGGCAGC TCTGCCCCTT 900
ACATCACCCC ATCCTGAGCC CAGCCGGATG TGGCTAAACC ATCCCCCTGC CTTCCCAAAT 960
TGTGGCTGAC GGTTGCTCAG GCAACCGCCT GCCAGACTGG GGAGATTAGC TGAGGAATGT 1020
AGCTGGGCCA GTTTGAACTG AGGCTGGGGG AGCCCTTGGG GGTCTTGGGT TGATTCAATT 1080
CACCCTCTCA GGGAGGCCTC TGTAGAGATG GGGTGCCCAA GGGCAGGCAT TCTCCCTGTT 1140
CCCAGTCTGA GGCTGCATCC CCAGGCTTGG CCCAGGCTGC AGAAAGGGAG TGTGTGTGAA 1200
CACTGAGCGC GGGGCTCAGG GCATATGTGT GTTGTGTGCT GTGCACCTCT CTGAGTGTGA 1260
TTGGAGGGTG TGCCGTTTAC ATCCTGGAAG GGGACTTGAG GCCCCTGTCC TCACCAGTTT 1320
CTGACATCTG ACTCTGGACC CCTTGGTGGC TTGGTCCCAA GATCCCTCTG GATCCTGCTG 1380
TGCTCTCTGG AGACACCACC TGCCCTACTC ATGGCTTATA GGATATATCA TTTATCTCAT 1440
CTGAATCCAG GATGAGATAA ACTTTCCTAC TCAAACACCT ACTGTGGCTT CTCAATTCAA 1500
AATGAGGCCC AGCTCCTCAC CCTGGCGTTC AGGGTCCTCC ATGATTGGCC TCAACCTCCC 1560
TTCCCTCCAG TCATAGCTCC CATGGCTTTA GCCAACCTGG GCTCCTTTCT GTGCCCTGGA 1620
CAAACTGTGT TTATTGACCA CCTTGCTTTG CTCCCCTGGG TCTTTTGCCA CAAATCCTTC 1680
CACCCATCTC TACCTATCCT TCTTGGCTCT GCTTAGATGC CGCCTCTTCC AGGAGGCCTT 1740
TCCCCTCTAC CTGGCCCCCT CCCCTGGACC CCCTCTTGTG GCCTTGACTC TTCCCTTATT 1800
CCCTCATTCC CTCTTCCTCA CCCTCACTGG GACTAGGAGG TCCCTGAGGG CAGGGCAGAG 1860
TCTTCATCAT CCTTGTACCT CTAATAGTGC CAGCCTGGGA CCTGCTTTGT ACTGGCAGGG 1920
AAAAATCCCC TGTGAATGAA GCTGAATTAA CACTTATGGC CAGCAGAAGG GCAGGCTTTG 1980
TTTTGTTTGT GCCCAGTCTC CTGGAATAAA GATAGGAGGT TTAAGTCTGA GCTTCTGCAC 2040
ATTGTAGCTG CATGGCCTTG AGTAAGCAGC TGTATCTCTC 2080
|
