| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26118 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:2875190-2876390 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr6:2875662-2875674 | AGCCCCAGGGCA | + | 6.11 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_09418 | chr6:2874486-2877653 | CD14 | | SE_10371 | chr6:2874228-2877934 | CD19_Primary | | SE_12023 | chr6:2874284-2878075 | CD3 | | SE_14917 | chr6:2874411-2877460 | CD4_Memory_Primary_7pool | | SE_16773 | chr6:2874244-2877530 | CD4_Naive_Primary_8pool | | SE_19481 | chr6:2874428-2877685 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20305 | chr6:2874272-2877558 | CD56 | | SE_38162 | chr6:2874697-2878717 | HUVEC | | SE_52689 | chr6:2874287-2877643 | Small_Intestine | | SE_53546 | chr6:2874486-2878627 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCTCCCCATC CCAGCCCTCC CAGCTTCTAC TCGGGGGTTC TCTCTGGCGA CTGGGCTCAA 60
TAAACAGGAA TCGAGCCACG CCCCTAAGAC AATGGACACC GATGAGCCGT CCCCGCTGGT 120
TCACCTGTAT TTACACACCC AGTTTCACAT CCAGTTAGAC ACTCTGTATC GTTATTGTCT 180
AATCTTAGGC ACACACTGTA TTCCTAGACC CATTGGTCTT TCCCTGCCCT CCCCCAAAGG 240
CAAAATGCAT TTAGGGTCCC AGAGATCCCT GGGGAGACAC GCAGCGGAGG TGACCTAAAC 300
CCAAAGCAAT GGTCTACGGA GGTGACCTAA ACCCAAAGCA ATGGTCTGGC CCCCTCTCCC 360
TCCTAAGCCT TCCAGCTAAG GGTTCTGCTC TTCCGGGGTC AGGGCAGGCC CCGGGCCGGT 420
GCGCTAATCC GGCTAGGAGG CTTCGGGCGA GGCAGGCTGG AGACGCCAGG GCAGCCCCAG 480
GGCAGCGGCT CCTGTCCCCA AGTCCTCGGG CCCTCCTCCA GCCTCCCTTC GGCGCAGGAC 540
CCTGGGGGAG CTCGTCCCCA CCGCCAAGCC GCTCGCCCTT CCCCGTTCGC CGCCCGGAGG 600
TTCGGGAAGG AGACACACCC GGGCCAGGCG CGGTTGCTCG CGCCTGCAAT ACCAGCACTT 660
TGGGAGGCGG AGGCGGGCGG ATCACCTGAG GTCGGGAGTG CGACCAGCCT GGCCAACATG 720
GCGAAACCGT GTCTCTCCCA AAAATACAAA AATTAGCTGG GCGTGGTGGC ACGAGTCTGC 780
AATCCCAGCT ACTCCGGAGG CTGAGGCAGG AGAATCGCTT GAACCCGGGA GAGGCTGCAG 840
TGAGCCGAGA TCCCGCCATT GCACTCCGGC CTGGGCGACT AGAGCGGCTC AAATAAATAA 900
ATAAATAAAT AGAAGTCACC CCTGTCCGAA CCTGGCTGAA CTCCAGGCGT TCCCCACCCG 960
CAATGCTGCG GGGTGCTGCC CCAGGATGCA CCCCTCCTAG GAGACGTCCC GCTTCGGAGA 1020
TCCCAGCTAC CCGCTCCCTC CCCCAGGCCG CCTCCCCAGA AGCCTCCGAG CAGTTGGGGC 1080
GCATTCGTGT TTGAAAAACA CAAGAGGAAG CGCCTGCAGC GCTCGGTTTC CCCCGCGGGG 1140
CAGCGCGGGC GCGGGGTGCG CGTGGGCGGG CGGCCGGGGT GGGCAGGGGA CCGTGGGCGG 1200
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