| Tag | Content |
|---|
EnhancerAtlas ID | HS176-25694 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr3:23201180-23201910 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr3:23201495-23201509 | TAATGACGTGTCAG | - | 6.16 | | PAX6 | MA0069.1 | chr3:23201679-23201693 | TTCATGCATCAGTT | + | 6.22 | | TBX20 | MA0689.1 | chr3:23201234-23201245 | AAGGTGTGAAG | + | 6.32 | | TBX21 | MA0690.1 | chr3:23201234-23201244 | AAGGTGTGAA | + | 6.02 | | ZNF263 | MA0528.1 | chr3:23201474-23201495 | GGAAGAGGAACAGGAGGGAAG | + | 6.09 | | ZNF263 | MA0528.1 | chr3:23201471-23201492 | TAAGGAAGAGGAACAGGAGGG | + | 6.26 |
|
| | 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 |
| GH03I023159 | chr3 | 23201090 | 23202141 |
|
Enhancer Sequence | GAGAGACTCT GTCAAAAAGA AAAGAAAAGA GAAAATACAT TCTAATATAG CTATAAGGTG 60
TGAAGCTCTT ATCTGCTGAG GTTGTTCTTC TACCACAAGC AAGAGCCAGC AGGGTTCTCA 120
CCATCCCTTT TAATATAAGG ATCTGTCCCC TAGATTTACC CCATAAGCAG TGTCTATGTT 180
GGACTACTAC AGTCCTAATT TTTTTTTATC AACAGAAAAT ACCAGCTTTT AATCAAATGC 240
ACAGAGAAAA TGTTTTAGAT AATGAGGATA TTCCCCGGTT TGTTTTAAAT CTAAGGAAGA 300
GGAACAGGAG GGAAGTAATG ACGTGTCAGG GACAGCATAA CCTCTATGAC TAAGGATAAA 360
GAGGGAAAAC CTTCTTGCCC TCAAAGTGAA ATCCCCTTCT ATTTTAGGAA ACACTCCTTT 420
ACTTTAAAGA ATCTCTCAAA TGAGTCACTA GGGTTAGATC ATATTCTTCT GGGACATTTA 480
CTTTCCAAAG GATAAAATTT TCATGCATCA GTTAGAAAGG AAAAAATATA ATCTGGCAAA 540
TAGGAGGCAG AACAATCCCT TTCCAAATGC TCTGTCTGTT CTGTCCTCTT AAGTCAACAG 600
AGCACAGCTA AATATGGCAG ACAATAAAGA TCTCAGTTTT GTGAAGATAA AAAGATTCAA 660
ACCTGGTCAG GCGCAGTGGC TCATGCCAGT AATCCCCACA CTTTGGGAGG CCAAGGCTAG 720
AGGATCACCT 730
|
