| Tag | Content |
|---|
EnhancerAtlas ID | HS098-01163 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:29575270-29576880 |
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 | GCACACACCC ACCTCCCCCT TAGGTGCAGG CTTACCACTA AATATGCCCT GTACCTTTGC 60
TTGTAAATGC ACGTCTATAC ACCCACGGCT TCACAGCGCC TGCCCGGGAG ACCTCCCCTT 120
TCCGACACCC ATGCCCACCC TCATGCACCT CTGCCCCAAG ATGACTCTTG CTCACGTGCA 180
CACTCACGCA ACTGCAACCG GTCATCTGAC CTTAGCGGTC CCCACTCTCA TTTTACAGGT 240
GAGGAGGTAA GGATTCAGAG AGGGCAAGTC ACCTGCCCAA AGTCACAAAG GGACTTAGAG 300
GCTCAGTGGG AAAAAGATCC CGGTCTTCCG CCTCCCATTT GAATACTTGA AACTCAGTAC 360
CAGGCTGTCC TGTCATCTTA GAGCCATGAG TGCACGTGTG CACACACACA CACGCACACC 420
TGCACACACT CACACGCACA CCTGCATGTG GACACATGCA TGGGGAGGTG TGGAGCCCCT 480
CCCACCAGGG AGACCCCTCC CACACTCCTC CAGAGGCAGC TCTGCCCCTT ACATCACCCC 540
ATCCTGAGCC CAGCCGGATG TGGCTAAACC ATCCCCCTGC CTTCCCAAAT TGTGGCTGAC 600
GGTTGCTCAG GCAACCGCCT GCCAGACTGG GGAGATTAGC TGAGGAATGT AGCTGGGCCA 660
GTTTGAACTG AGGCTGGGGG AGCCCTTGGG GGTCTTGGGT TGATTCAATT CACCCTCTCA 720
GGGAGGCCTC TGTAGAGATG GGGTGCCCAA GGGCAGGCAT TCTCCCTGTT CCCAGTCTGA 780
GGCTGCATCC CCAGGCTTGG CCCAGGCTGC AGAAAGGGAG TGTGTGTGAA CACTGAGCGC 840
GGGGCTCAGG GCATATGTGT GTTGTGTGCT GTGCACCTCT CTGAGTGTGA TTGGAGGGTG 900
TGCCGTTTAC ATCCTGGAAG GGGACTTGAG GCCCCTGTCC TCACCAGTTT CTGACATCTG 960
ACTCTGGACC CCTTGGTGGC TTGGTCCCAA GATCCCTCTG GATCCTGCTG TGCTCTCTGG 1020
AGACACCACC TGCCCTACTC ATGGCTTATA GGATATATCA TTTATCTCAT CTGAATCCAG 1080
GATGAGATAA ACTTTCCTAC TCAAACACCT ACTGTGGCTT CTCAATTCAA AATGAGGCCC 1140
AGCTCCTCAC CCTGGCGTTC AGGGTCCTCC ATGATTGGCC TCAACCTCCC TTCCCTCCAG 1200
TCATAGCTCC CATGGCTTTA GCCAACCTGG GCTCCTTTCT GTGCCCTGGA CAAACTGTGT 1260
TTATTGACCA CCTTGCTTTG CTCCCCTGGG TCTTTTGCCA CAAATCCTTC CACCCATCTC 1320
TACCTATCCT TCTTGGCTCT GCTTAGATGC CGCCTCTTCC AGGAGGCCTT TCCCCTCTAC 1380
CTGGCCCCCT CCCCTGGACC CCCTCTTGTG GCCTTGACTC TTCCCTTATT CCCTCATTCC 1440
CTCTTCCTCA CCCTCACTGG GACTAGGAGG TCCCTGAGGG CAGGGCAGAG TCTTCATCAT 1500
CCTTGTACCT CTAATAGTGC CAGCCTGGGA CCTGCTTTGT ACTGGCAGGG AAAAATCCCC 1560
TGTGAATGAA GCTGAATTAA CACTTATGGC CAGCAGAAGG GCAGGCTTTG 1610
|
