| Tag | Content |
|---|
EnhancerAtlas ID | HS116-10286 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr14:20957010-20958320 |
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: 3 | Chromosome | Start | End |
| chr14 | 20957499 | 20957600 | | chr14 | 20957600 | 20958200 | | chr14 | 20957012 | 20958201 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I020488 | chr14 | 20956733 | 20960426 |
|
Enhancer Sequence | AGAATCTTGA TCTGTTACCC AGGCTCTGTG GAATGCACTA GTATGATCAT AGCTCTCTGC 60
ATCCTTGAAC TCCAAGGCTC AAGCAATCCT CTTGCCTCAA ACTCCTGAGT AGCTGGGACT 120
ACAGGCACAT ATCACCACAC CCAGCTGATT AAAAAAAATT TTTTTTGTAG AAACAAAGTC 180
TTGCTATGTT GCCCAGGCTG GTCTCGAATT CCTGGCCTCA AGTGATCCTA GCACCTCGGC 240
CTCCTAAAGT ATTGGGATTA CAGGCATGAG CCAACGTACC TGGCCTTATA TTATTTTTAA 300
ACTTATTTAT ATAGAAGAAT CAAATTTACT CTGTGCAACT TTGGAGAGTT GACTAGGACA 360
GGAGAGCCCA CTCAATATTA GAAAAAGAGC TCTACAAAAA AGACATTGTT ACGTTACATT 420
CCTGAAATGT TGAAATAGGG GCTAGAGGAA TATTTGACAA AGCTGTAGAG AGAAATAGTT 480
GACCTTATGA CCTCTAAAAT TCTTTTCAAG ATATTTTATC TGCAAAAACC TGAATAGCAA 540
CAACTATAGT TCCACAACAC TCTAGTTCTA CAGAAGGAGG GTGGGATGTT ACACTGTGCT 600
TTCATGTTTC AATAATTATA TATCTATCCA TGCATGTCCA CTTCTGCTTG ATGCCACTGA 660
AGTGGGACCT GAGGAGCTGG GGTGCTAGGG CAGAAAGAGT AAGGTCTGTG CCCGATCCTA 720
GACAAAAGTG GAAGCAATTC ACTGCTTCAT CCATCACGGA AGGGCAACTC TTTAGCTTAG 780
CAAACTGAGA AATTTTCAGG CTCAACACCA GCAGGAATTC AATTTGCAGC AAGATAGACC 840
TCAGGGGATT GAGGCAATGA TTCAGAGAGG ATGGGTGGGG TAGGGTTACA CAGGAACTTT 900
AGAGAAAGAA TCGTTTGTGG GTGGAAGCCT TGGGCAGAGG TGCACTCAGT AGAGAAGAAA 960
GCCATTTGTT CCAGAACAGC AGTTTGAAAG GGGTGTGTTT TGTGTGGGCA ATGGTGTATG 1020
AGGAAAGGGT TTGTGGGGAA GAAGCGTGTG GGGCTACTAA CAGGCACAGA AACACTTGTT 1080
GAGAAATGTT GTTCATAGGG GGATTGCTTT GCTGGGGCCC AGGAGCAGGT GGTTTGGTGC 1140
AGTGAAAGAG GCCAGAGGGG CAGAAAGAAG GGTCCTAGCT GTGGCCTTAA ACACACACAT 1200
ACACACACAC ACACACACAC ACACCAAAAA GCAAGGAAGA ACCCCTTATC CTCTCAGCCA 1260
AGATAAGCAA GCGCTGTTAC CAGCTAGGTG TGCTTACTAT GGATTTTATA 1310
|
