| Tag | Content |
|---|
EnhancerAtlas ID | HS129-00821 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:33418990-33420320 |
Target genes | | Number: 24 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:33420123-33420138 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_35956 | chr1:33418362-33420740 | HMEC | | SE_64575 | chr1:33418511-33420826 | 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 |
| GH01I032952 | chr1 | 33418289 | 33420570 |
|
Enhancer Sequence | AAAAGCTAAT AACATTTTCT GGGATTTATT CTACAGTTTG CTTGTTTATT TGAATGTACA 60
TGAGATGTTA ATCATAGCAA CTCAAGTTCT CAGGTTTATC ATAGAGTCTG CAAATTGACT 120
TGAGAATGAT GCTGAAAATA TAAATGACAA TGTATCCCCT ATGTTATATA ATACAGGCTG 180
TATTAAAACT CTTTTCAGAA AGAACAAAGT GAGAACAGGT CAGTCTATGA ATGCAAATGA 240
TTCATATCCT GTAGGAGTTC TGGGCAAATT TACCCCACCT AGCTGCAAAA TAACTACTAA 300
AGATAAACAA CGTGTCTCCT CAAGACAGTG ACTAGCTTGT TATTTTGCAT TAAATGGGAA 360
AGTTACTGGA TGACCTCAGA AAAGCACTAA GTCAACTTCT AAAGATACAA ATTAAGTGGA 420
CATCCAGTAG GGAGCCTTGA ACACTTCATC ATCCATTCCT ACCTCACATG GCAGAAGTAA 480
ATGTTTATTA ACATTCCCCC AGCCCCCACT TCTTTTTTTT TTTTTTTTTT TTTTTTGAGA 540
CGGAGTTTCA CTCTTGTTGC CCAGGCTGGA GTGCAATGGC GTGCTCTCGG CTTACTGCAA 600
CCTCTGCCTC CTGGGTTCAA GCGATTCTCC TGCCTCAGCC TCCCAAGTAG CTGGGCTTAC 660
AGGCGCCCGC CACCATGCCC AGCTACATTT TTTGTATTTT TAGTAGAGAT GGGGTTTCAC 720
CATGTTGGCC AGGCTGGTCT CGAACTCCTG GCCTTCAAGT GATCCTCCTG CCTCAGCCTC 780
CCAAAGTGCT GGGATTACAA GTGTGAGCCA CCGTGCCCAG CCCACTTTTT TTTTTTTCTT 840
GAAAAAGAAG AACATTGGAT AGGATCAACA ATGTCAATTT TGAGTGTGTA ATTTGGTGCC 900
AAGGAAGTAA AATAACCCCA AATTACTCAT GAATCCACAG CAATCTATTA CTACGACACA 960
GAATTACTCA GGGCACGAGA TTTGGCATTC CTGTTTTTGG GTACCTGGTC TGAGCTCTTG 1020
CCTCTGACTC ATGCTGCATG ACATGAAGCT ATTAAAATCT CCAAACCGGC CTGGTGCAGT 1080
CACTCACGCC TGTAATCCCA GCACTCTGGG AGGCCGAGGC AGGTGGATCA CCTGAGGTCA 1140
GGAGTTCAAG ACCAGCCTGG CCAACATGGT GAAATCCCGT CTCAACTAAA AATACAAAAA 1200
TTAGCCAGGC ATGGTGGCGC ATGCCTGTAA TCCAGCTACT CGGGAGGCTG AGGCAGGAGA 1260
ATTGCTTGAA ACTGGGAGGC GGAGGTTGCA GTGAGCCAAG ACCACACCAC TGCACTCCAG 1320
CCTGGGCAAC 1330
|
