| Tag | Content |
|---|
EnhancerAtlas ID | HS129-02687 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:183163560-183164920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr1:183164111-183164122 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr1:183164111-183164122 | CAGCAGCTGTC | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_35834 | chr1:183163338-183165417 | HMEC | | SE_64350 | chr1:183163237-183165340 | NHEK |
|
| | 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 |
| GH01I183194 | chr1 | 183163373 | 183169370 |
|
Enhancer Sequence | GTGATAGCAA AAAATCTTTG CCTAATCTCC TTGTACAAAA AAAGTATTGT TCACAAAAGC 60
AGTAAGGATT TAAAAAGGAA GATTTATTGT TTTTTTTTAA GGAATCAATG AAACATAAAT 120
TTAAATAATT GAAAAATCAT GGTTTATACT TCAATTATCT CCAAAAGGCA TTTTAGTACA 180
AATTAGAATC TCCTTTTTAA CTTCTCTTTA TTCAGACACA TCATAGAAGG TTTCTTTCCT 240
TTTGGTCCTC TTTGCTTCAG GTATTTACCT CTGGCATCCC TGGAATCTCT GATTCCCTTT 300
ATTTCAACTG CTTCTTAGAG GGGCATAGGA TACCTTTTTC TAGGCCATGC AAGAAATGTC 360
CAGAGAACAC TATGCTCTTT GAATAACAGT TAAATGTCCT TTCTATGCTG GAATGCTTTT 420
CTTTGTAGGT AACTTCACAG AAATGTATAA CCCTTTATTT CTGTGGTCAG AAGAGTGTGG 480
AGTTCCATGG AGGTGGTTGC TGTCATATAG AATCTTACCA CAATCACTTC CTGAGTCTAT 540
GCTGCAGCTG ACAGCAGCTG TCTTGCGGTA GAGCCTTTGA CAGTGCCAGC TATAACTCTA 600
ATGTCCTCAG TTTGCCTTCC CTTTCACCTG TGAGCTTACT CAGACTGAAC CCTCAGTTTT 660
ACCTTTACCC TCCACTCCTT TGCTAGTCAG ACAAAACTTG GTGTCCCCAG TTTCCCTGTT 720
CACTGGGACT TTCTTCCCCC TCCTCATTGT CTGCCTGGGC ACTGGTGTCC CAGTGGAGTG 780
TCAGGGGAAG ACATCTCCAG GTGTGAACTC CTGATGGAGT CCTCACCAGG CTGAGTCATC 840
TACAGTTCAC ACGGGTACAT TCCCAAGTCT AGGCTGTGAT ATAATGTACT ATGAACTCTC 900
GGTGAAACAG GTGTCTCCTC TGAAGCCATA ATCATTCAAA AGGAAATGGC AGTGATCTGA 960
GTTTCACTGA CTCTTGATGA CTTTGGAGTA TTCAGAGTTG AAAAAACTGA CCCATACTTT 1020
ATGATTCAAA ATTGCCTGTG AGATTAGAGA ACTGAGCTCT GTCATTCCTC TCATCCTAGC 1080
ACTTCCTGCC TCAGCCTTAC TCACATTGCT TGGACATTTA AATGTCAACT GGTGCCGTGC 1140
CCTTTATTTA AATGAAACAA ATGGATCAGG CAGGATATGG TATCAGTTTT CTGGCTGTGG 1200
TGGCTTAAAA TGTGGCTATG AAAAATTTGC AAAAGAAGCC TAAATTCAGC TAAAAGCCTT 1260
AGTGAGAGAA GTACCATTTC AGTTTTCTTA TTCTAATTAG GGAACATATT GTGACATTCT 1320
TTAAGAAGAT AAAACTAGAA GCAGATATTC ACACATTAAA 1360
|
