| Tag | Content |
|---|
EnhancerAtlas ID | HS133-09527 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr14:78304750-78306220 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat4 | MA0518.1 | chr14:78305722-78305736 | GTTCCGGGAAATGG | + | 6.3 |
|
| | 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 |
| GH14I077838 | chr14 | 78305241 | 78305390 |
|
Enhancer Sequence | ATTTTTGAGA CAGGGTGTCA CTCTTGTCGC TCAGGGTGGA GTGCAGTGGT GCAATCATGG 60
CTCACTGCAG CCTGGACTTC CCAGGCTCAG GTGGTTCTCC CACTTCAGCC TCCCAGGTAC 120
CTGGGAATAC AGGCACGTGC TGCCATGCCT GGCTAATTTT TTGTATTTGT AGTAAAGATG 180
GGGTTTCACC ATGTTGCCTA GGCTGGTCTC GAACTCCTGG GCTCAAGCTA TCCACCTGCC 240
TTGGCCTACC AAGCTGCTGG GATTACACTC GTGAGCCACT GCACCTGCTC CCGCTCCAGT 300
TTTTTGCTTA TGGAAAAGAT CTTTACCCCC TAACCCCCAA CATGTTATGG GATGAAGGGG 360
GATGTCTCTC TGCTGTGCCT GGCCACAGTG CAGACTATCT AAGCCACTAT TCATTCAGCC 420
AATTGTTCAG TGATATTTAT TGAATGCCTA CTATGTTCCA GGCACTGTGT GGGGTGCTGG 480
GTGTACAATG GTCTGTTCTT GGGAGGACAA GAGGTAATTC ACAATGATGG GACTCAAAAG 540
CACATCCGCT CCAGGAGGAT AGGGGACTTG TTTGTATTGC TTGCTGCTGT GTCTGCAGCA 600
CTAAGAACAG TGCTTGCCAC ACACAGAGTG GTCTCAGTGT ACACTTTTCA GGAAATCACT 660
GTGGGTCTAA GTAAACAAGG TCATTTCAGC TCTTGCTGAG TGCCCTAAAG GAGATAAAAT 720
GTAGTCATGG GATAAAGAGG GGCTGAGGGA GAGTCTGGGA AGGGCTCTCT CGCATGATGT 780
TTTTCAGCTG AAACTGAAGA ATGATCAAAG GACTAGCAAG TGAAGGGCTG CGGGGAGACT 840
GTTAGAGGAA GAGGCAGGGC CGGCCATGTG ATTACGAGGA CTAGTGCAAA ATGAAAATGC 900
TGGGCTCTGG CTGGGCGTGG GAAAGCCTCC CTTCCCATGG CCCTGCTGCC CCAACCTTCA 960
AAGGATGGGC AGGTTCCGGG AAATGGCAAG CTGTGTGCTG GGGCGAGCTC AGGATCTGGA 1020
TGGGGGTGGG TGAGAGGTGC CTGCCAAGCT GTGTGCTCAG CTTGCTGTGG CTGTTCTAGT 1080
TTAGGATGGG GCTGGATAAC ATGTGGCACC TGTGTGACCC CAACCCTCCC CGTGCCTGTG 1140
TCAAGGCCAC CTGCAGGGTG GAGAGCAGTG CACAATGCAG GCCTCCCCTT CCCGGTGCAC 1200
TGCTTGCAGA GAGCAGCAGT GATGGCAGGT AGAAGTAGGG AGATGGGGCC CGATGTGGTG 1260
GCTGGCCTGT AATCCCAGCA CTTTGGGAGG CCGATGCAGG TGGATGACGT GAGATCAGGA 1320
GTTTGAGACC AGCTTGGGCA ACATGATGAA ACTAAAAATA CAAAAATTAG CCAGGTGTGG 1380
TAGTGCGCGC CTCCTCAGCT ACTTGGGAGG CTGAGGCAGG AGAATCGCTT GAACCCGGGA 1440
AGTCGAGGCT GCAGCAAGCT GAGATTGCAC 1470
|
