| Tag | Content |
|---|
EnhancerAtlas ID | HS062-10786 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr22:36519560-36520750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr22:36520119-36520131 | GCTGACGTCACC | + | 6.14 | | CREB1 | MA0018.3 | chr22:36520119-36520131 | GCTGACGTCACC | - | 6.14 | | CTCF | MA0139.1 | chr22:36520209-36520228 | CAGCGCCACCTCCTGGCTC | - | 6.06 | | Mafb | MA0117.2 | chr22:36520114-36520126 | AAACTGCTGACG | + | 6.02 | | Nkx2-5(var.2) | MA0503.1 | chr22:36520319-36520330 | CTTGAGTGGCT | - | 6.62 | | Zfx | MA0146.2 | chr22:36520566-36520580 | GAGGCCGAGGCGGG | - | 6.01 | | Zfx | MA0146.2 | chr22:36519865-36519879 | CCCGCCCAGGCCTC | + | 6.08 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_00529 | chr22:36518990-36520719 | Adipose_Nuclei |
|
| | 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 |
| GH22I036123 | chr22 | 36519201 | 36520770 |
|
Enhancer Sequence | CAGTCACAGG CTTTCAACAT GGAAGGTGGA GCTGCCTGGA CGCTGTGTTT TTTTTCTGTT 60
TGTTTTTTTG AGACGGAGTC TTGCTCTGTC ACCCAGGCTG GAGTGCAGTG GCATGATCTG 120
GGCTGATTGC GCCTCGGCAA AATCTCGGCT GACTTGCCTC CCGGGTTCAA GCGATTCTCC 180
TGCTTCAGCC TCCCGAGTAG TTGAGATTAC AGGCGCGCAC CACCACGCCC GGCTAATTTC 240
TGTATTTTTA GTACAGACGG GGTTTCATCA TGTTGGCCAC GCTGGTCCTG ACCTCAAGCG 300
ATCCGCCCGC CCAGGCCTCC CAAAGTGCTG GGATTACAGG AATAAGCCAC CGCGCCCGGC 360
CAGACGCTGT GTTTTCCTGG CACTCCACTT CATGAGCAAA ACTGTCACAG AGTAGTATTT 420
CCCTGGCTCC ACCCCTCCGG CGCTGCTGGA TTCCTGAACC TATTCACTTC TTCTGAAGTG 480
CTCTCAACTT GGCCTCCCTG GCTCCTTCCT GGTGCAGACA TTTACTCTTC CTGCTCCGGC 540
TTTGTGCCTC TGTAAAACTG CTGACGTCAC CAGCAGCGGC TCCGACCGCC TGTCCTCCAA 600
GGTCCCGGGC TGCGGCTGCG CAGCGCCGAC AGCACGATGC GTGTGCCGAC AGCGCCACCT 660
CCTGGCTCTG CCGAGGCTGT TGGCAACACG CAGGGCTCGC AGTGCGCCCG CTTTTCTACT 720
GCAGCCCTCA AAATTCAGCA CGAGGCTTGG CTAGGGGAGC TTGAGTGGCT GACACTGTGG 780
TCTGGTTAGT TTCCATTCTG ACCCATGCTA GCCGTCTTTC AGATTCTAGA ACTCAGTTCT 840
TCTCCGGACC TCCCTCCCAG CCACAAGTCT TTGAATATGC GGCCTGCAGC TGGGCTCCCC 900
TCATCCCCGC TCTTCTCCCC AACCTTCTTC ATCATCCCTT GGCCGATCTT GAAGACTTAG 960
CGGAGGCAGG GCGCAATGGC TTACGCCTGT AATCCCAGCA CTTAGGGAGG CCGAGGCGGG 1020
AGCATCACTT GAGGTCAGGA GTTTGAGACC AGTCTGGCCA ACATGGTGGA ACTTTGTCTC 1080
TACTAAAAAT ACAAAAATTA GCTGGGCGTG GTGGCGGGCA CCTGTACTCC CAGCTACTGG 1140
GGAGGTTGAG GTAGGAGAAT CGCTTGTACC CGGGAGGCAG AGGTTGCTGT 1190
|
