| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06103 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:95496320-95497720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr12:95496592-95496603 | AAATCACAGCT | + | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_36502 | chr12:95496115-95498227 | HMEC | | SE_65110 | chr12:95496509-95498232 | 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 |
| GH12I095102 | chr12 | 95496201 | 95498305 |
|
Enhancer Sequence | TTGGTATCTG GTGGATGCTT CAGGTACCCC CAAGAAATTT GCTTGTTCTG ACTGCTAGCT 60
GCGAAGCATT TGACAAACCC TAGACACAGG TATTTGTCTT CTCCTGTCAT CCTGTATGTC 120
AGGCAGCAGT AGCCATTGCA TTTCAGAGGA GTAGCACACC CCAGGATGAC TCTTGTGGTC 180
CTCTGATTTT GGGAAGTCAG ACATTTGGTT TGAGTCCTTG ACATTCATGG ACGTAAGCAA 240
AATTATAAAG GTTGTCAGAA ACACCTAGGT TCAAATCACA GCTCCACTGC TTACTACTCG 300
TGTAACCTTA GATGTGTTAT TGAACCTCTC TGAGCCTCCA TTTTTCTAAT CTGGAAGATC 360
AAGATAATAT CCACCCCACA AAGTTATCAT AGAACTTAAA AGAGAAAATA AATATAAAAC 420
GAAACATGAG CACTGTGACT GATGCAGAGT AATAAATGAT TCTGGCCACT ACTCCACCTG 480
CTCCTAAGAT CCTAGTTGAT TTCAGTGGTA TGGACAATTG GAAACAGACT GCCTGGTTTC 540
AAATCCTGGC TCTGCTAGTA TAGCTGAGTG GCTTTTCTCA GCATAGAATG GGTATAATAA 600
CGACAACTTG CCTTACAGGT TGCTGTGAAG ATGAAACGAA GTACTACACA TAAAGTCTTT 660
ATGATGGTGC CTGGCATACA GTAAGTGTTA CAAAAGCGTT TGCTTCTATT TTTATTAGAT 720
CAAAGGTTAG GTCTGAGAAG ACAGTGTCTC ATTATTTAGA TTGTGCAGTG GAGCATGCTA 780
TGACTATTGG CATCTCTCCC TTCACCAGTC AAACCTTCCC AAATACCCAC TTCCGCCACT 840
CAGTCAGTAA CTCAGTAATG TATTTTTATG AGTCATAGAG TTTCAGGTTT CCTCAGCACT 900
TGAATTACAT TATGGCAACA TATTAAGTCA CTGCAGGTTC CGGTCTGGGG CAAGGTGGTA 960
TCATAAATAA TAATGGATTT CTTTTCCCGC CCTCCCTCCA TTCTTTCTGA GATGGAGTCT 1020
TGCTCTATCA CCCAGGCTGG AGTGCAGTGG AGTGATCTCG GTTCACTGCA ACCTCCACCA 1080
CCCAGGTTCA AGTGATTCTC CTGCCTCAGC CTCCCAAGTA GCTGGGATCA TAGGCACATG 1140
CCACCATGTC TGGCTAATTT TTTTGTATTT TTAGTAGAGA TGGGGTTTCA CCATGTTGGC 1200
CAGGCTGGTC TCAAACTCCT GACCTCAGGT GATCCACCCG CCTTGGCCTC CCAAAGTGCT 1260
TGATTACAGG CGTAAGCTAC TGCACCCAGC CCATAACAAT GGACTTAAAA GCAAAAGACT 1320
TCGATTTGCA TCCTGGCTGT GTCAAATATG TATCCGTAAG ACAGCAACTC CATTTTTCTG 1380
TAATTTAGTT TCCTAATTTT 1400
|
