| Tag | Content |
|---|
EnhancerAtlas ID | HS095-08750 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr14:20956650-20958460 |
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 | TATTTTACAT TTTTTGGTCC TTTTTAGTTG TGATAATTAC TGAGACCCTT GAGCAAGTAT 60
CATTGATATT TTTCTCATTT TCATTTTTCT GATTTAAAAA GGCTTAGAGA AAGGTTATCT 120
GACTTTTCCA ATACCACACA GCAAAGGAAT AGCTAAGCTA TTCCTTCAGG CTCAGAACTT 180
TTGTCACCAT AGCATTAGAT CTACATAAAG AGATGGGGAT GGAGAATGTG TAAAAAGGCA 240
TCACGTTTAG GTTGAATGAA AAGCCAGAGA GTAGTTAAGT TTGGTGGTAA ACAGAAGATG 300
AAAGGAGGTA GTGAAGAACT GTCTTCTATT AATATTATTA TTATGATTTT TTTAAGAGAT 360
AGAATCTTGA TCTGTTACCC AGGCTCTGTG GAATGCACTA GTATGATCAT AGCTCTCTGC 420
ATCCTTGAAC TCCAAGGCTC AAGCAATCCT CTTGCCTCAA ACTCCTGAGT AGCTGGGACT 480
ACAGGCACAT ATCACCACAC CCAGCTGATT AAAAAAAATT TTTTTTGTAG AAACAAAGTC 540
TTGCTATGTT GCCCAGGCTG GTCTCGAATT CCTGGCCTCA AGTGATCCTA GCACCTCGGC 600
CTCCTAAAGT ATTGGGATTA CAGGCATGAG CCAACGTACC TGGCCTTATA TTATTTTTAA 660
ACTTATTTAT ATAGAAGAAT CAAATTTACT CTGTGCAACT TTGGAGAGTT GACTAGGACA 720
GGAGAGCCCA CTCAATATTA GAAAAAGAGC TCTACAAAAA AGACATTGTT ACGTTACATT 780
CCTGAAATGT TGAAATAGGG GCTAGAGGAA TATTTGACAA AGCTGTAGAG AGAAATAGTT 840
GACCTTATGA CCTCTAAAAT TCTTTTCAAG ATATTTTATC TGCAAAAACC TGAATAGCAA 900
CAACTATAGT TCCACAACAC TCTAGTTCTA CAGAAGGAGG GTGGGATGTT ACACTGTGCT 960
TTCATGTTTC AATAATTATA TATCTATCCA TGCATGTCCA CTTCTGCTTG ATGCCACTGA 1020
AGTGGGACCT GAGGAGCTGG GGTGCTAGGG CAGAAAGAGT AAGGTCTGTG CCCGATCCTA 1080
GACAAAAGTG GAAGCAATTC ACTGCTTCAT CCATCACGGA AGGGCAACTC TTTAGCTTAG 1140
CAAACTGAGA AATTTTCAGG CTCAACACCA GCAGGAATTC AATTTGCAGC AAGATAGACC 1200
TCAGGGGATT GAGGCAATGA TTCAGAGAGG ATGGGTGGGG TAGGGTTACA CAGGAACTTT 1260
AGAGAAAGAA TCGTTTGTGG GTGGAAGCCT TGGGCAGAGG TGCACTCAGT AGAGAAGAAA 1320
GCCATTTGTT CCAGAACAGC AGTTTGAAAG GGGTGTGTTT TGTGTGGGCA ATGGTGTATG 1380
AGGAAAGGGT TTGTGGGGAA GAAGCGTGTG GGGCTACTAA CAGGCACAGA AACACTTGTT 1440
GAGAAATGTT GTTCATAGGG GGATTGCTTT GCTGGGGCCC AGGAGCAGGT GGTTTGGTGC 1500
AGTGAAAGAG GCCAGAGGGG CAGAAAGAAG GGTCCTAGCT GTGGCCTTAA ACACACACAT 1560
ACACACACAC ACACACACAC ACACCAAAAA GCAAGGAAGA ACCCCTTATC CTCTCAGCCA 1620
AGATAAGCAA GCGCTGTTAC CAGCTAGGTG TGCTTACTAT GGATTTTATA CATTTTAGAG 1680
AAAATTTCTA ATGCCCATTT GTCCTGAACT TTTTACTTGG AATATCGTTA AGTTTACGGA 1740
AAAGTAGAAA GGATCATGTA ATGAACACTA GTGTACCTCT CACCTAAACC ATCAATAGTC 1800
AATAATCTGC 1810
|
