| Tag | Content |
|---|
EnhancerAtlas ID | HS020-42466 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr8:11297250-11298350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr8:11297764-11297779 | GAGCCCAAGGTCAGG | + | 6.42 | | RARA(var.2) | MA0730.1 | chr8:11297598-11297615 | TGACCTTCTGGGGACCT | - | 6.11 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_32248 | chr8:11297181-11298254 | Gastric | | SE_58515 | chr8:11271776-11367112 | Ly1 | | SE_60559 | chr8:11246636-11318640 | DHL6 | | SE_61363 | chr8:11297105-11326062 | HBL1 | | SE_65314 | chr8:11296805-11299418 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH08I011441 | chr8 | 11297621 | 11297810 | | GH08I011440 | chr8 | 11297841 | 11297990 |
|
Enhancer Sequence | TTCATCCTGG CACTGCATAA ACCACGTGGA AGACTTTATT GCCCCTTTTC TCTGTCTTCC 60
AGGTTGGCAA GGGGAACTTG TGGGTGTGAA TGAAGAGAGA AAACAGAAAG GAGGGTCCCT 120
GCTCCCCTGT GCTGAGTGCC CAGGGCCCCA TCCCAGGGAG TTGGCTGATG GACCAAAGCC 180
CGGGCAGAGG CGTGTGTGAA TGCTCTGAAT TCCGGACTCA GCTAGAGAGG AGAGAATCCC 240
ACAGCTCCAG ATCATGCTCT TCCTAGCTCC CCTACTTCCT CAAGCAATGC CCTCCCCCCA 300
CTCCCACCCA GGCTACTCGG CTGCCTGGAA GGTGAAACCT GGGGGCTGTG ACCTTCTGGG 360
GACCTGAGCA GCCTAGAACT GCAGCTGCAC AACGGCCACT CCCCTGAGCC AGTGTCCCAG 420
GAGCAGCGAG ACTGGGCCTC GCCTGGAGGA GTCAGGTGGC CGCAGCCCTG CCTGCCACAG 480
CCAGAGAGCC ACACATCTCC AGCTCCGCCC CGGGGAGCCC AAGGTCAGGC CGTCTTAGCT 540
GGGAGTCGCA CTAAGAGGCT TGGAGGATCT CCATCAGCCT TGAATCCCCA ACACATTAGC 600
CTGAAGGAAA ATCTGATCTA CTTGCTGATC CCTGGGGGGC GTCAGGAGTG ACAGTCATTT 660
CCTTGAAAGC TGAGAGGGAG AGCTGACCCC TGAGAGCTGT TAGGATCCTC CCAGCCTCAG 720
AGATCAGCCA CAGTCAGGCA ATCATTCTGC CTTTTAGCTG GTCTTGCAGG AGGCGGGAGC 780
AGATTAAGAC GATGCTTCCA GACCCAGCAC TGCCTGCCTC TGGTTGAGGT GACATTGACC 840
ACTGCCTCCT GGGAGAGCTG CTAGGTGGTC AGAGGACAGG TTAGAGTCTG CCTTCTCCTG 900
CAGTCAAAAC TCCCTTTAAG TTACAGAAAA TATCCACACG ACTAAGGGAA TTACAGATTT 960
CTAATCGATT TCCTTGGCCA CGTGAGAACA AACAACACAT TTGCACTTGA GCCTAACAAA 1020
TCTGTAGGAA GGGCTTGCCC AGGTGTAGAG AAAACCACCT TCTGGGCTTA AAATATGACA 1080
GAAAAGGTTA TGCAAATCAC 1100
|
