| Tag | Content |
|---|
EnhancerAtlas ID | HS179-11474 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr14:20957420-20958320 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr14:20957489-20957504 | TGACCTTATGACCTC | - | 7.63 | | RARA | MA0729.1 | chr14:20957486-20957504 | AGTTGACCTTATGACCTC | - | 8.07 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 20957499 | 20957600 | | chr14 | 20957600 | 20958200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I020488 | chr14 | 20956733 | 20960426 |
|
Enhancer Sequence | ACGTTACATT CCTGAAATGT TGAAATAGGG GCTAGAGGAA TATTTGACAA AGCTGTAGAG 60
AGAAATAGTT GACCTTATGA CCTCTAAAAT TCTTTTCAAG ATATTTTATC TGCAAAAACC 120
TGAATAGCAA CAACTATAGT TCCACAACAC TCTAGTTCTA CAGAAGGAGG GTGGGATGTT 180
ACACTGTGCT TTCATGTTTC AATAATTATA TATCTATCCA TGCATGTCCA CTTCTGCTTG 240
ATGCCACTGA AGTGGGACCT GAGGAGCTGG GGTGCTAGGG CAGAAAGAGT AAGGTCTGTG 300
CCCGATCCTA GACAAAAGTG GAAGCAATTC ACTGCTTCAT CCATCACGGA AGGGCAACTC 360
TTTAGCTTAG CAAACTGAGA AATTTTCAGG CTCAACACCA GCAGGAATTC AATTTGCAGC 420
AAGATAGACC TCAGGGGATT GAGGCAATGA TTCAGAGAGG ATGGGTGGGG TAGGGTTACA 480
CAGGAACTTT AGAGAAAGAA TCGTTTGTGG GTGGAAGCCT TGGGCAGAGG TGCACTCAGT 540
AGAGAAGAAA GCCATTTGTT CCAGAACAGC AGTTTGAAAG GGGTGTGTTT TGTGTGGGCA 600
ATGGTGTATG AGGAAAGGGT TTGTGGGGAA GAAGCGTGTG GGGCTACTAA CAGGCACAGA 660
AACACTTGTT GAGAAATGTT GTTCATAGGG GGATTGCTTT GCTGGGGCCC AGGAGCAGGT 720
GGTTTGGTGC AGTGAAAGAG GCCAGAGGGG CAGAAAGAAG GGTCCTAGCT GTGGCCTTAA 780
ACACACACAT ACACACACAC ACACACACAC ACACCAAAAA GCAAGGAAGA ACCCCTTATC 840
CTCTCAGCCA AGATAAGCAA GCGCTGTTAC CAGCTAGGTG TGCTTACTAT GGATTTTATA 900
|
