| Tag | Content |
|---|
EnhancerAtlas ID | HS147-28919 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr3:101682730-101683990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr3:101682903-101682917 | GTGAGTCATTTCTT | - | 6.55 | | TCF3 | MA0522.2 | chr3:101682754-101682764 | AGCAGGTGTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_55900 | chr3:101681056-101684485 | u87 | | SE_67850 | chr3:101681056-101684485 | u87 |
|
| | 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 |
| GH03I101964 | chr3 | 101682844 | 101683244 |
|
Enhancer Sequence | CCTTGCTTCT TTCATTTTGT GCATAGCAGG TGTTCAATAA ATCATTTTTA ATTGAAGTAG 60
ATAGCTGTCT ATTATGAAAA TGAGAAATGA ACTTGACAAG AACACTGCTT CTTCTCTCTG 120
CCCTCCTTTA TTTGTCATCA TTAGCTCAGA GATCTCATTT TACCTCCAGA TTTGTGAGTC 180
ATTTCTTCCT CTTGCCTCAC CCATAGCTAT TTTAATTCTT TGAAAACTGG AGTTAGTTAT 240
CCTTTTCAAG CCTCCAGTGA GTGCTGCGGT GACCTGATTT CCAGTTGCTG GGTGCTTGCT 300
TTGGGCAAGT GTACCTCCAC GATTGAAATC TTCCCTCCAC CCCGAGCTCC TGAGGCTCTC 360
TCCACTCTGT CATCTGTTTC AGAAGCAGTT TTTGTACCAC CTTGCTTTTA CCTTTGAGGC 420
CATACCCACT GTTGGTTACT TCATCCTGTG GCTATGTCTA TACAAGTGAA ATTAAGTGCA 480
TAATGAAGTC AATGGTGGGT TTAATTCAGG CCACTTTTGC CTGACACTTC TTTCTTTTGC 540
TGTCAGCTCA TCACCTCAGC ACCCCCAACC CACTTATTGT TTGGAGGCTG GGATCTGCTA 600
TGCCACAGGA GTATTTTCTG AGCCTTGTCA TTTACTTCAA ATGATGGAAG ACATTTTCTT 660
TCTTCAGGAA TTATGAGACC TAATCCACCT GGATTTAGCA AATGGGTTGT TCTTCCTGCT 720
GGTTGCTAAA AACCATCACG TATTCAGTTT TCGACAAACA ATTGTTGAGA ACTTACTAGG 780
TACAAGCAAT AATACCAACA CAATTATTGT CTTCAGGGAG TTCTCTAGAG GCTGCGGGCG 840
TGCACTGCTC AAATCCACTT GCGTGAGAAG CTCATGAGGA GGGTAGTTAG CTGACAGTTT 900
CCAGCTGCGG CCCCTCTGGC TCTGCCCCTG CATTCACGCT GACAAGTCAC AGACTTCTGG 960
GGATTCTTCT AGCTAGTAAC TGAATGTGGT AGTTGTATGG TACCATGGTC AGGCTATTTC 1020
TGGCTGGCAT GGGACTCCTC TAATGAGGAG TCTTTGCTTG AGGCCTCCTG GTCGGCCTGG 1080
CTCAGACTCA GTGCTGCAAT GCCGTCTGAC TCCTACTACC CAGTCCTCCT CCTTCCCTCC 1140
TATTCTGAAG GCCCTCCCTG CCCATGCTGG TTGCCCCTCC CCAAATCCTT CACAGGCGTT 1200
TCTCCCAAGA AATCTCCTGC ATGACTAATT TTGTCTTGGC ATCTTGTTCG TAGAAGAGTT 1260
|
