| Tag | Content |
|---|
EnhancerAtlas ID | HS037-12048 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr14:81851850-81853450 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr14:81853153-81853168 | TGAACTTTGCTCTTT | - | 6.59 |
|
| | 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 |
| GH14I081385 | chr14 | 81852247 | 81853263 |
|
Enhancer Sequence | GGAAATCATA ACCCTATGAA AATAGCTGAA AAGAAGGGGA CAGGATGGGT AAGAGGCCAG 60
TTTCCTTGCC TATCTTGTTT AAAAAACAAC AAGCTGACTT CACTGAGGGC GCCATCCTTC 120
AAGTTCTACC TAACAGCTCA TTAGCCCCAC AAATGGGAGT CAGTCACTTA GTCATTCTGC 180
AGAAGGTTTC ATGTCCATCT TTTCTCTCTC CTTTCACTAG TCCAGCAAAT CCTAGGTGGG 240
CACCTACTAA GTTCCTCAAA CCATATTCTG GAATAAAGAA TAAATTAGAT AGACAAAGTC 300
TTTCCCTTTA TGGAGAAGAG AGATAATAAC AAGTAAACTA ATGCATATTT GACCCAATTG 360
CAGGTAGAGG CATGGGCTGT GAAGACATTT GAAGCAGAAA AAAGCTAGAG AGTGGAGGTG 420
GAGGGTTCTG GCCCCCCGCT GCAGAGGCGA TGCTTGAGCA GAGTTTGGAG TGAAAATGTG 480
GAGGAAAAGC TCTCAGGGCA GAGGGAACAG CCAGGGCAGC AGTGAACTGG CCTGGAACGG 540
CGAGAGAGGC AGTGCAATTA CAGCAGACGG AGCCCAGGGG AGAGGATCAG AGACGGCATC 600
AGCCCTGAGA AGGAAAGGCT CTGCTGAAAT TTATTCCTGG GTACAGCATC CTCTGAGACG 660
GACTCCACAA AGGTCATTAA CTACATTTAG AAGCACAGAA GAACAATTGA AGGTATTAAA 720
AAAAATAAAG CCTCTTCTGT TGCAGGGGGA ATTACATATG CATGCAAAAT GCAGTAGGGC 780
CTTGTCCACA TATTCACCAA AAGGGTTGGG ATATCTTATT CCACCCCCAC CCACCACTCA 840
CTACCCCCAT TAGCCAGAAT GAACAACATA ATAGAAATTA ACGGCGGGGC TAGTCTTCTT 900
CAGGATGAAG CCTCTCAGCT GTCACCCCTG CCTCCCTCTT AAATGGCTGA CATCATCTCT 960
GATCCTCCCC CAAACAAGTG GCTCTTTCTC TGGTCCCAAA TAATTAGTTT CCCCAGACAC 1020
AATGGGAAGG CCTTAGCCCA AGCTTTTAGG GAAGACGTTT GAAGCATAAG GGAATACTAG 1080
TGTTTTGCTT GGGCTATGGG ACAAAAGTTC CGGAAATGAA AGGGTTTTTT TGTTGTTGTT 1140
TGTAATTATG CACATCCTGC AGTATCTGCA TAATGGGTCC AATTCAGCCC TGGCCTTGCA 1200
GAAAAATTAC CATGTCCCTG GAGGAAGGTC AGCATATGAG TGAACAGGAA GCTTCATGCT 1260
GACAATAGTG CCTTAATTTT TTTTTCTTTT TAAATTTTAA GGATGAACTT TGCTCTTTTA 1320
GTCCATTTGT CTGCAGGCAT TTGCAGACAT GTTCTAAACA CACCCACACT TGTAAAATGT 1380
ACGTACTTAA AATCAGCCTT GGCTTTGAGA GAACAGTATA AAGATTTTGG ATGATAGATG 1440
GGCTGACTGC TATATTCTTC CCGGTACCTG GTGGAATTTT AAAGCCAGAG GAAGCCTTAT 1500
ATGTTAATCA AACTTTTTGT AACTAGAGAT AGTCAGGAAC ACTATTGGCT AAAGGACTCA 1560
ACGTGAATAA GACATGAGAT GGGTTTAGGT TCATTTTCAA 1600
|
