| Tag | Content |
|---|
EnhancerAtlas ID | HS191-11369 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr14:20957390-20958320 |
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 | GAAAAAGAGC TCTACAAAAA AGACATTGTT ACGTTACATT CCTGAAATGT TGAAATAGGG 60
GCTAGAGGAA TATTTGACAA AGCTGTAGAG AGAAATAGTT GACCTTATGA CCTCTAAAAT 120
TCTTTTCAAG ATATTTTATC TGCAAAAACC TGAATAGCAA CAACTATAGT TCCACAACAC 180
TCTAGTTCTA CAGAAGGAGG GTGGGATGTT ACACTGTGCT TTCATGTTTC AATAATTATA 240
TATCTATCCA TGCATGTCCA CTTCTGCTTG ATGCCACTGA AGTGGGACCT GAGGAGCTGG 300
GGTGCTAGGG CAGAAAGAGT AAGGTCTGTG CCCGATCCTA GACAAAAGTG GAAGCAATTC 360
ACTGCTTCAT CCATCACGGA AGGGCAACTC TTTAGCTTAG CAAACTGAGA AATTTTCAGG 420
CTCAACACCA GCAGGAATTC AATTTGCAGC AAGATAGACC TCAGGGGATT GAGGCAATGA 480
TTCAGAGAGG ATGGGTGGGG TAGGGTTACA CAGGAACTTT AGAGAAAGAA TCGTTTGTGG 540
GTGGAAGCCT TGGGCAGAGG TGCACTCAGT AGAGAAGAAA GCCATTTGTT CCAGAACAGC 600
AGTTTGAAAG GGGTGTGTTT TGTGTGGGCA ATGGTGTATG AGGAAAGGGT TTGTGGGGAA 660
GAAGCGTGTG GGGCTACTAA CAGGCACAGA AACACTTGTT GAGAAATGTT GTTCATAGGG 720
GGATTGCTTT GCTGGGGCCC AGGAGCAGGT GGTTTGGTGC AGTGAAAGAG GCCAGAGGGG 780
CAGAAAGAAG GGTCCTAGCT GTGGCCTTAA ACACACACAT ACACACACAC ACACACACAC 840
ACACCAAAAA GCAAGGAAGA ACCCCTTATC CTCTCAGCCA AGATAAGCAA GCGCTGTTAC 900
CAGCTAGGTG TGCTTACTAT GGATTTTATA 930
|
