| Tag | Content |
|---|
EnhancerAtlas ID | HS133-22360 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:53174470-53175630 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr3:53175027-53175038 | AGCCAATCAGA | + | 6.32 | | SRF | MA0083.3 | chr3:53174785-53174801 | TGACCATATATGGGCA | - | 9.15 | | SRF | MA0083.3 | chr3:53174785-53174801 | TGACCATATATGGGCA | + | 9.33 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09542 | chr3:53173777-53178723 | CD14 | | SE_43193 | chr3:53174020-53175908 | Lung |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr3 | 53174758 | 53175140 | | chr3 | 53174865 | 53175140 | | chr3 | 53174779 | 53175200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I053140 | chr3 | 53174418 | 53175816 |
|
Enhancer Sequence | GTAGGAGGGT GTGTATGCTG GTTGAGCATG TGAGCATGTG TGTGAGAGAC TGTGTTAGTA 60
CGTTTGTGAG GTGAAAGTGT GTAAGCATGT GCCAGCGTGA GTGATTGTGT AAGCATTGTG 120
TGGGTGTGAG TGATGCAAGT TAGTGCATAT ATGGCAGTGT GCAAATGAGT GTGTGTGTAT 180
GAGTACAAAT GTGTGTGATC ATATGCCTGT GTTCATGAGT GTGTGAGTGT GTGCATGTGT 240
GAGAATGTGT GTGAGTGAGG ATGCATAGGA GTACCTATGT GTGTGTGTTC ACCTGTGTTG 300
TGTGGTGTGC TTGTGTGACC ATATATGGGC AACTGTGTGC TGAGGGTGTG CATGCAGGTA 360
TAACTCTCTC TGGGTGTGAG TGAGAGAGAG AGAGTGTATG AGTGTGTGTG CATGAACTGA 420
GCATGCGTGT GCATGTGTTT CTGTGAGTGG TTGTGGTACT GTGTGTATGT GTGCCCTGAG 480
TCACGTGCTA GGGTAGGTGG CCCCAAGGGA AGGGAGAAGG GAGAATTCTC TAGGCTTACT 540
CACTATGGCT CAGGCACAGC CAATCAGAAA ATATTTCAAA ATAGACTTGC TTGCATTTGT 600
CATGGCAACT TCCTGCTACC CAGTGGCCAG AAGGCTTCCT AGAGTTGCAG CTTGTCAGGG 660
ACCTCTCAGA GGCACAGACT GTTGGAACTC AAAGGGGTCT TGAAGCTCAT CTCCCCAAAG 720
ACCTCATGTT ACAGGTGGGG AGACTGAGAC CCAGGGTCAC ATAGCTGTTG AGGGCAGAGC 780
TAGGCTTGGA ACTCAGGCCT TCTGTCTAGT GTGCTTGTGC CTCCCACCAA CATAAACCTT 840
CTGCCTCCCT GGCCGTCATT CATTCATTCA TTCATTCATT CATTCATTCA TTCAGCAAAT 900
GTTTACCAGT CCCTATTAAG TGCTGGGTTC CAGGGTACAA ATCCTGCCTC AAGGAGCTTT 960
CCTCCCAGTG CAGGGAGGTG GGCCGAGAAT TCTAGATCCC GATAAGTACC CTGAAGACAG 1020
GAAGGCAGGG TGATGTGATG TCAAGGCCTG CTTCAGCTGG GGGTCAGGGA GGGCCTCTAC 1080
AGAGTGGCAC TGTGGCTGAA GCCAGGTGGA TGGAGCCAGC ACCTCACAAC CAGCTATCTA 1140
GACCCATTTC CTAATCAGCC 1160
|
