| Tag | Content |
|---|
EnhancerAtlas ID | HS133-17491 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:113693460-113695090 |
Target genes | |
SNPs | | Number: 7 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr2:113694153-113694164 | CATGAGTCACC | - | 6.62 | | JUND | MA0491.1 | chr2:113694153-113694164 | CATGAGTCACC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr2 | 113693868 | 113694223 | | chr2 | 113693817 | 113694227 | | chr2 | 113693621 | 113694612 | | chr2 | 113694749 | 113694985 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I112936 | chr2 | 113693868 | 113694223 |
|
Enhancer Sequence | CATAATTGGA TGAGGCTTTT GGGACCCTTG GGAGGTTGTG AGTATATTTT GCATAATGGA 60
GGAATAGAAA TAGTTTGTAC CCAAAAGACA GATTGTGATA GATGCAAATT TGTTGACACT 120
TATCCCATTG AGAGATGTCC TCTATATGTT CTCCTCTTGA ATTGGTGCAG GTTCTGTGAC 180
TGATCAATAG AACATGGCAG AAATGAAGCT TTTGCCAGTT TCTGGGCCAA CGTCTTAAGA 240
GACTGTGAAC TTTCAATATT CCTCCACTCT TCTGTAGGTT GTGATACTTG CTCTTGGAAT 300
CCAGCTGCCA TTCTGTAAAG AAGCCCATGC AGCCCGAGAA GGGGCCATAG GAAGAGGAAT 360
TGGGGCCCTT GGTCAACAGC TCCCTGTCAA TTGTAAGCAC CAATTTGCTG GCCACTTCAG 420
GGAGCCATCT TCTGTGTGAC CCTCCAGTCT CAGTTATACT TCCTGACACT GCGGGAACGG 480
AGACGAGATG TCCTCATTGA GCCCTGCCCT GCCCAAACCA CAGATCTTGA ACAAAATACA 540
CGAGTGCTTT TTTTTTTTTT TTTTTTTGAG ACGGAGTCTC ACTGTGTCAC CCAGGCTGGA 600
GTGCAGTGGC ATGATCTTGA GTCACTGCAA CCTCCACCTT CCGGGTTCAA GTGATTCTCT 660
TGCCTCAGCC TCCGGAGTAT CTGGAATTAA AGGCATGAGT CACCGCGCTC GACCACGAGT 720
GCTGTTTTCA GCTACTGTTT TGGGATGGTT AGAAATGCAA CAGTAGATAG CAGAGATATT 780
TTGATTTTTG TAATTTTTTG CTGTAACCGT CTTCTACTAC ATTAAATTAT CTAAAACATG 840
TGAAGGAGGT AGAAAAAGAT GAGGTGGCTG CACATCCACT TCTACAACAA GGTGACCACA 900
GAAAGTAGCC ATGAGTGAGA GGGAAGGGGC AAAGACTAGG TTAAGTCAGG GAGTGAAGTT 960
GGGCTCAGGG AAGACTTCTG CTCTTTTTCA TTCTTCTTAA CAATCAGGGA GTCCAGGCAG 1020
AAGTGGCCTG TCCCATCTCT TCTTCCAGGT GCTCATTTAG ACTCAGTTAA CATCTCTCCC 1080
CACCTCCTCC CTGTACCCCT CTTCTTTAAC ACACGAAGGA CCTTCTGGAG ACTTCTCTCA 1140
ACTAAGCCCC ACCAAGGGCT TACTTCTGTC TATGGCCCCT TGGCTACTTG ATGATTTCAT 1200
GTTCTTTATT TTTTTTGGGC AAATATTCCT TAATGTTTTT AATTTTTAAT TTGTTAGGAT 1260
CATTATGTTT CATAATGCCA AAAACAGATG GTCAACTTAG GGAAAAAACG TATAAAGCAC 1320
TTAGGAACAT ATGTAACAAT GAGTACTATG ATGCATATTG ACTGAGCACA TAATACATGT 1380
TAGGTACTCT CTCTCTCTCT GTGTATTGCA CTTAACTCTT ACAACAACCC CAGCACACAG 1440
ATAAAGGAAC AGGGGCTTTG AGGCTGAGCA AATTGCCCAA GGTCCCATGG CTGATAAGTG 1500
GGAGAGAGGC TGTAGTTTTC TGTCCCAAAG GCCATGGTCC TAACTATTAT ACTATGCATC 1560
ATCTTAAGCA CTATGAATGT TTAATGTCTG TCCTTCCTGT CTTTTATGTG TGTGTATTTA 1620
TAAATATAGA 1630
|
