| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00722 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:25406350-25408160 |
Target genes | | Number: 21 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:25406994-25407015 | CTCCAGTTTCACTTTTAGCCC | + | 6.03 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGATGGTCTC GATCTCCTGA CCTTGTGATC CACCCGCCTC ATCCTCCCAA AGTGCAGGGA 60
TTACAGGCGT GAGCCACTGC GCCCGACCCA GCAGGTGACT TTTTAGAGAC ATTCAGGGGT 120
TCCCTGGCTA GTGCAAAAGG CACAGAGACC CTTCCACCAC CATGTTCTGT GCTACCTTCT 180
CCCCTCACTT TCTCAATGGA GCATTTCTTC CTGAAGTCCC CAGCCTGCCC CTCCAGGATA 240
CAAAGCTCAC CAAAATTTGG TGGCTCTATC TAGGCTCTTG GCCATCAAGC CAAAAAAAAA 300
AAAAAGTAGC TTCAGTCCTA ATGCCACATA CAAGCTGGCC TTAATATCAG AGGGAGATAT 360
CTTTCTCTTT AAGCAGAGCA GACTCTTTGG GAATGCATCT CTGGGTGGCA GAGAGAGCCC 420
AGAGGAGCCA GAAAGGCCAA GGCCTATGAA TCCCAGGAAA TAAGCTCTGT TGTTCCTGCG 480
GACTCACAGG GAGAGAGGAG AACACTCAGC CTCTTCCTCC CTGACAAGTG AACACACTTC 540
ACAAAGACTT AATCATGGGT GGAAAGTCCT CACTCCTCCA CCTCTTCGGT CATAGGCCAC 600
TTTAACTCTC ACCTCGACCA GAGAGACAGT CTTCCCACTG GTCTCTCCAG TTTCACTTTT 660
AGCCCCTGTA TTAGGCCAGG CTGGGCTGTG CTGACTCAGT GGCTGGCTTG AAGGAACAAA 720
GATTTCTTTC TGTCCATTGC TGGTCAGGTG CAGCTCTGAT CCGTGTCATC CTCACTCTGA 780
AACCAGGGTG GATGGAGCCT CCTTCTAGAA CACTACAAGT TGTTTTGGAA GAGGGGAAGG 840
AGATGTTGCA AAATCATGCA ATGCCCTAAA GCTTCTGCCC AAAAGTAGCA CATGGCACTT 900
CTACTCAAAT TTCATTGGCC ACAGCAAGTC ATATGACTAA ACCTGATGTC AATGAGGTAA 960
GAAAGCAGGA TCCTCCCACA GGGAAGAGAA GCAAATAGCT GAGAACAAAC GAAATCATCA 1020
TGTCCCCTGC TTCAAACCTC CACTTTTCAC TCATGCTTAG GATAAAACCC CAGCTCCTGC 1080
CAGGCCTGGC CCTGCCTCCT GCACTCCTCA TTCTCAGTTC CTCTCCTGCT TCCCGCTTGC 1140
TCCAGCAGCC TGCCAAATAT GCAAGCTGGT TCCCGCCACA GGGCCTTTGT ACAGGCTGCT 1200
CCTCAGGCCC AGGTCAATGC TTTAACCCAA CTCTCCCCAG GCCTGCCTTT TCCCATAGTT 1260
TAGAGTTCAG CTTAAACGTC ACAGAAGAGA GGCTTCCTTG ACCATCCCAT TATTCTCTCC 1320
CATATTACTC TGTTTATGCC CTTTCTAACA CTAATCAAGC TGGAATTCAC TTGTTTCTGT 1380
AACAGTTTTA TTATGTATTG TGTGTTACAC TCACACACCA GAACACAAGC TTCTTAGGAG 1440
TGCATGTATC TGTCCTGTTT GCCACGGTAC AGCTCTCTCA GCAGGAGCTC AGCAAATGTT 1500
GGTGGCACAA ATGAAAGAAT TGGGTTGAGA CAGGAGGAGC CAAGCCTGGT CCCGAGAGCC 1560
CAGTGCATTT CAGCATCATG AACCCTTCCC ACACCCAGGT GGCATTGCAG GGTGTGCAGT 1620
GTGGAGCCCA AGCCTCCCTG TCCTTGCCCA CCCACGTCAC TTCACTCACA ACCAGAAGGT 1680
ACATTATGTG CTGGCAAAAA AACTACAAGC AGATGTGATC ATTTTATCAG ATGGCCACTC 1740
TGGACTGGGA GCTGTGGTCT GCATCCTAAC CACAGTGCCT GGAAGCCTGT GAGGTGGGTG 1800
TCATGATCCT 1810
|
