| Tag | Content |
|---|
EnhancerAtlas ID | HS133-09343 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr14:64389200-64390920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr14:64390214-64390229 | ATTTAATCATTAATT | - | 6.76 |
|
| | 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 |
| GH14I063921 | chr14 | 64388640 | 64390965 |
|
Enhancer Sequence | AGCCCCTCCA AGTGTTTCTT AAGATAGCCA TGTGTTAGGG CTAGGTGCAG TGGCTCACGT 60
GTATAATCCT AGCACTGTGG GAGGATAGCT TGAGCTCAGG AGTTTGAGAC TAGCCTGGGC 120
AACATGGCAA GACCCCATCT CTATAAAAAA TACTCATGTG TTATAATATT TATTTTGAGA 180
TATATTAATA TCTCAGAGTT TATCATTTCA TCGCTATTTT TTGCCAGGCC CTTCTTATTC 240
CCTGTTGTTT CAAGAGTAAG TCATACATGT AAATTGTCCG ATCTATTTAG ACAAGTATTT 300
CACAAAGTGA GATATGTGAA GCCCTGAATC AGAATCTCTG GGAGTTGGGA TCCAGAAACC 360
TGCACTTAAA CAATAACCCT GAGTAATTTG CTGGCATTCC AAAATGTAAG AACCCTGGAT 420
TTATAATCAC AGCACAGCTC TGTTTAGTGC AGTCTGGTTC TTTTGCACTC AGAAGTCAGA 480
GGTGCTTGGA CTGCTGCCCC AGTAGAAAGT GTTCAGGCTC ACATACCTTG ATTTTTCAAA 540
AGAAAAGTGT TCAGTTTTAT GTGGTAGTTA AAAGGTAGCA AGGAGTAACA AATATGTGTT 600
AAAATAAATG TAGTCATTTC TTTATTTCTT CATTCCGTAG ATATTTATTG AGCAACTTAG 660
ATGAATCAGA AGAGTGTGAG AAGGAGGAGA GACAAATAGC ACCCAACTTC TAGACTTTTA 720
TCAGTATTGT GGGCTTATTT TCATGTGCTA AAAATACAAG ACTTGCTTAC GCAGAGAGCC 780
GGGAGCTATG TTCCAGTGAG GGTGGAAACA AAAGCCTCAG TATAAGACTG TCAGGTGTTT 840
ACACAAGGGT GTGGTTTGCT CATGTGGCAA CACGAGGTTG CTGGACTCCA CATGCTGAGG 900
CTCAAAGTAG AAATCACTGA TCTTATGTCA CATATTTTCC CAACAAACTA AGTACTTAAA 960
TCTGTATGTT GATTGAGGAA AAATAACAAA CTCCTGCTCC CTCCTTCCCT AGCCATTTAA 1020
TCATTAATTC AATAAATGTT TTCTAAATTC CTATAGCATG AAAGCTCTGG GGTAGGTGCT 1080
GCAGGCAAAA TGAGGAGCAA ACTCAGACAT GGGTCATGTA CTGTTGGAGC CCATAAGCTA 1140
ATGAGGAGGC AGAAGTTGAT CAAATAATCT TATAGATATT AGCTAATATT TTATTAAGCT 1200
TTATTAAGAT ATAATTTGAC ATCAAATTCA CATACAATGC AATTCACCCA TTTAAAGCAT 1260
ATGATTTAGT AGTTTTCAGT ATACTCACAG AGTTGAGCAG TCATCACATT GGATTTTAGA 1320
ACTTTTTTTT TTTTTTGAGA CAGTGTCTCA CTGTCACCCA GGCTGGAGTG CAGTGGTGCC 1380
ATTTCAGCTC ACTGCAATCT CTGCCTCCTG GGCTCAAGCA ATCCTTTCAC TTCAGCTTCC 1440
TGAGTAGCCG GGACTACAGG TGTGTGCCAC CACACCTGGT TAATTTTTTG TTTTTTTTTA 1500
TTTTTGTAGA GACACGGTTT CACCATGTTG TCCAGGCTGG TCTTGAACTC CTGGGCTCAA 1560
GCAATCCACT CACCTCAGCC TCCCAAATGT TGGGATTACA GGCATCAGCC ACTGTGCCTG 1620
GTCAAAAAAA GTATTCTTTT CCTACTGACT TTTCTTGGCA TGCCTGTCAG AAATCAATTG 1680
CCCATAAGTG GAAGAATTTA CTTCTAGATT TTCAGTGCTA 1720
|
