| Tag | Content |
|---|
EnhancerAtlas ID | HS132-00806 |
Organism | Homo sapiens |
Tissue/cell | Melanocyte |
Coordinate | chr2:65086070-65087380 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr2:65086613-65086624 | TTTGACCTTGA | - | 6.14 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_00723 | chr2:65084051-65089167 | Adipose_Nuclei | | SE_09303 | chr2:65083825-65093604 | CD14 | | SE_10494 | chr2:65084599-65093132 | CD19_Primary | | SE_11245 | chr2:65083337-65093393 | CD20 | | SE_53747 | chr2:65084570-65093131 | Spleen | | SE_57888 | chr2:65086422-65087223 | VACO_503 | | SE_62791 | chr2:65045447-65101119 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 65086460 | 65086681 | | chr2 | 65086968 | 65087262 |
|
Enhancer Sequence | AATGCAGACT GACAAAGACA TCCTCTTTTG TCTTCCTTCC TCTTTGAGAC TAGAATGTAT 60
TTTCTGAGCT CTCCTTTGCT TTGCTTTTCT TTTGGGTACC ATGACCCAAG GTACAGTATA 120
AATACGTCAG TATTTGTAGC CTGTAGAAGG TCACTCAAGA ATGTGCATTT GTAACCATCT 180
GGGGAGAAAA TAGGCTTTGT CAGTGAGTGT TTCCTCTGGT ACACTTATTA CACTCTAGCA 240
AGTATCATGT ACGGGAGATG AAACAGGCAG CTGAAAGGTG TCCCGCCTGT GCACCTTCCT 300
GCTGGCCCAG CGTCTATTTC CAGCCTCCTC TCCCAGGGTT GCTGAAACCC GGAGCTGATT 360
TCTACATTGG AAGTTAGGAG CTGCAGGAAA CGCCTCGTGC CGTGCCGGGG ACGTGGAGGA 420
AAGCCAAGTG CCCTTGATAG GCTCCTCCTC TGGAGCTAGG GAGTTCCCTG GATGGTGGCA 480
GGAGGAGCTG CGGTTCTGCA GCTGCTGCGG GCGGGGCAGC TGCTGGCGGC ACTGTGTCTT 540
GGGTTTGACC TTGACCCCTG GGCAACACAG GGAGACTTTC ACACCCTTCA CCCTTGCATC 600
ACTCCACTCA GAGGTGCGCA GGGCCCAGCC CCAGCTACAG ATGAGGAGAC TGAGGCTCGG 660
AGGCTCTCGG ACCGCCCAAG GTCTCTGGGC AGATCAAACG GTGGAGAGAG GCCAGAGCCA 720
AGTGTCTTGG CTCCCGGGCT GGGAGAGGCC CCGGCGTGGC CCTCTGGAGG CCGCCGTCTG 780
CGACTGCCCG GGCGCCCTGG GGCGGCAGCC TGGCCTCCTG GGCTCGAGGC AGGGGGCAGA 840
GGTGTCCCGG CGGGGCCGGG GCCGGGACAC GAAGAGGGAG GCGAGCAGGG GCTAGGAACT 900
GGAGCCGGTT TGTGCTCGCG CGCCTGCAGG CCCTTTGCCT CGGGCACCCC CGCTCCAGCC 960
CAGCGGGGGC GGCGCCGAGA GGGGCCCATG GCCCAGACGG AGGCTCGGGC TGCGTCCATT 1020
GGCGGCCGCA GCCCCGGGGC GGGAGGGGGA GCGGCCCGGC GTCGGGTTAC CGGGGACCAG 1080
CACGGCAGCT GGCCCCGGGA GGCAGCCGCG GGGTGAGGGT GCATTCTTGG ATTCCTGGCC 1140
GGGAAGGGAA ACCAAACCGC ACTTGTATCC AACGCAATCA ACAAACATGA TGTGTCAAGT 1200
GCTGTATTGC ACTTGAGCGG GTGTAAAATG GTAGAGCTGG GGTTCCTGCC CAAACGTTCG 1260
TCTAATTGAG GAAATAAGAA ATCCACAGAG AAGAAGAACG CTGGAGATAC 1310
|
