Tag | Content |
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EnhancerAtlas ID | HS133-26042 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:326850-328570 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr6:328512-328525 | CTCATTTGCATGT | + | 6.54 | ZNF263 | MA0528.1 | chr6:327326-327347 | GGAGGAGAGTGAAGGTGGAGG | + | 6.03 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_10946 | chr6:327141-344260 | CD20 | SE_32457 | chr6:326363-334033 | GM12878 | SE_43503 | chr6:326454-334344 | MM1S | SE_52667 | chr6:326804-329317 | Small_Intestine | SE_53696 | chr6:327428-328784 | Spleen | SE_58945 | chr6:285215-361947 | Ly3 | SE_61974 | chr6:285209-337654 | Toledo | SE_62393 | chr6:286339-359703 | Tonsil | SE_67150 | chr6:326454-334344 | MM1S |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I000326 | chr6 | 326986 | 328930 |
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Enhancer Sequence | GTGGTGTGCT GTATCAGATG TCATTTAAAT GGAGAAGACA AATGGGATGT GCAAAACAAG 60 CTGTCACCAT CAGAATGACT TTGTGCAATG GGACTGTCTA GACCGAGGCT TGGCACGCTT 120 TGGCTGTCAA GGCCCAGGGA ATATTTGGGG CTTTGGGGAC TTCTGCTGCA GCTACTGTAG 180 CCTCCACCAT GAGGTGAGGG GCCACAGACA ATACGTGAAT CAGTGGGCAC AGCTGTGCCC 240 CGTGAACATG GGCCCTAGTT CACCCACCCT GGGCTTCGCT GTTGGGCAGC AGGAGCATTA 300 CTGAGAGGAA ACTAAGAGCT TCCAGGAGCC CAGCCAGGTC TGAATCTTGG GGCTGGGTAG 360 CCCCCAGTTT AATGCAGCCC CAGAAATGCC CAGCATCTTT GCCTTGTCTT TGCCTGTCAT 420 GGTTTTCTGT GTGGGAGCGT GCACTCACCA CGTCCAGCAG AGCCCCATTT ACAGCTGGAG 480 GAGAGTGAAG GTGGAGGCCG GCCCGCACTG GACGGTGACT CCAGGGCTAC CTGCAGGTGC 540 CGTGGCCAGC CTGGGAGCAG TGCTGTCAGG GCGCATTGGG TTGGTGGCCA CATGTTTAAA 600 ATTCTGAAAT GGCATGTCCC TCCTCATGCA TTCCTTTCTT CATTTGGAAC CGTTTACAGG 660 AGAGAGGTGC CAGGAGACTG ATAGATGATG ACCACAGCCG TGGGAGTTCG AGGAATCTGG 720 GGTCTAGTGA GAGAGACTGG CCCTTCACAC GCAGTGCCAG TCCTCTGTGC CAGGGCCATG 780 CGCCTGTGTG CTGCTGGTGG TGTGGGGGCC CAGCGTGGGG CTGAAGTCTG CTAAGGGGGA 840 GGCCGAGGAG GTGAGGGAAG GCTCCACAGA GAGCCTGGTG GGTATGTCAG GGAGGTTTTA 900 CTGAGAAGAG CCACGCAGAA AGCCTATTCC AGAGAGAGAA AACCACAGGG ACTTGGCAGG 960 ATGGCCGGGA GCAGGGAAGC ACAGAACATG TGGGGAGACT AACAGCAGCC CAGGGTTGCT 1020 GGAGTTTGAG GAGCGAGGGG TGGTAGGAGG GAGAGATCAT GGATGTGAGG TCAGGAAGGG 1080 GGTTGTGGAC AGATGCTGAA GCACTGTGAA AATGGGTCTT CTCTACTTTG CAGACAGAGA 1140 GGAGCCACTG AATATTTTTC AGCAGCTGAG ATGTGTGATC AGATAATGTT TGTAAGAGAT 1200 AAATTTTTCC CTGGTGATAC GTACAGAGAA CACTCCTAGA ATATCTGCTG CTGATTTCTA 1260 AGCAGCAGCT TTCACTCATG GCAGTTTTTT GAGATGGGTT GTTCAGGCTT CACCTTCATT 1320 AAGTAATACC ACGGAATGCC TTGGTCCCAA GTGACTGCTG AAACTGGCCC AGTTTTCATG 1380 AGTCACAATT GTGTACATCA GCAAGTCCTG CAGCTGAACT GAAAGCACCC GGTAGGGCTT 1440 TCAGTGGTGA GACGGAGCTA GAGTGAATCT CCCTCACTGC CTTCCCATAA CCCAGCCCGT 1500 ACTGGCTGGA GGAAATCCAA CATTCTGACC GTGCCCACTT TAGCCTTGCA CTGAAATATC 1560 TTGAACAAAA ATAAGCTTTT GAGTTCTCAT CTGTTGATCT GACAAGTCAA ATGCATGTCG 1620 GTTTTTGACT AACCTGAAAG AAGTCACAGG TGTTGGAGGT TTCTCATTTG CATGTTGTCT 1680 CACAGTATCA AACCAGAGGC TAAATCTTGT CTCTCCACTC 1720
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