Tag | Content |
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EnhancerAtlas ID | HS133-08155 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:122600950-122602300 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAX | MA0058.3 | chr12:122601285-122601295 | ACCACGTGCT | + | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_23525 | chr12:122600876-122602205 | Colon_Crypt_1 | SE_24216 | chr12:122600905-122602116 | Colon_Crypt_2 | SE_32300 | chr12:122600870-122602245 | Gastric | SE_48379 | chr12:122600805-122602384 | Psoas_Muscle | SE_50423 | chr12:122600437-122602366 | Sigmoid_Colon | SE_52993 | chr12:122600870-122602436 | Small_Intestine |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I122116 | chr12 | 122600604 | 122603154 |
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Enhancer Sequence | AAACAGCTCA GAAAATATGG GGCACATGGC TAACGCGCAG GTTTTTAATT ATGAAATTTC 60 ATTAACAAAT GATGCAAATT GAAGTGAAAT ACCAAGTTTG CCTCTTGCAA ATCTGGTTTC 120 ATCTCCAGTC CGGAGGAGCA CCTTGGGGTC TGATTGGGGT TTACTCTTCT GGCGAGGAAA 180 CCTAGGACTC TGGCTTTAAA TGGTGCCCTG CCCAGGGGTC CCTGCCCCTG CCCCTGCCTG 240 AAAGTCCACT TATGGCTTGA ATCTGACAGG AAACTTAAGA ACATGCCCAA GAAGCTCCTA 300 AAACTCAGGA GCATGCCTCA CCATGCCCAG CATTGACCAC GTGCTGGGCC CAGGCCCTCA 360 TATCTGCTAT GGCTGACCCA GCTGTCCAGT GTGGTGGATG TGGTCACTGT TTTGCAGAAG 420 GTGGGCTGGG CCGGGCCAGC CTGGGTGACG AGGCCAGAAA TGGAACCACT CTGCTTTCTT 480 TGTTGGTTAG AAGTGGTCTA GACATGGTGG TGTCTGTCCT CTAGTGGAAG GCCTGGACAC 540 AGCCCATCCC AGGCAGGGTG AAGTCACCAT TGCAGGCAGG CACATCTTGC CTGGTATCCA 600 CTCCCTCAAG TTGCCCTATT TTTGGGTGGT CATGGAAATG ATTACTCCCT GCTTTTCACA 660 CAGAAAAGAC AAACATACAC CCTCACAAAC AAGCTGGCAC GCATGTGGGC GGAGCACCTG 720 CAGGCACTCG AACACTCGCA CACTGGAGTG TGCACCAGCC TTCCCGCCAC AGCCCTCGGA 780 TCCTACTTCT CCAACAGGAT GTTCTTTGAA TGTAAGAAAA AAGATGCCAA GAGATCCACG 840 AGGAGGATGG AGCAGGACCT GAAACCCCCT GGGGTTCCTC CATAGGAGAC TCTCTGCTCG 900 GGCAGGTGGC CCGACATGCA CACTGCCCCT CCTGTCAAGC CATTGGCAGT GGCCCCTCCC 960 GCGTGCCAGC TCCTCAATGA ACCTTTGTTC GTCTGTAGCC TGTTAGCTTT GGCTGCTGGC 1020 AGCCTGTGGG ACCAGGCCCA CATCCCAGGA CTAGCCGATA GAGACTGCCC TTTTGAAGCA 1080 AGTGAATTGG ACTCCTGGAA GAGTCATTCC TCCACTCCCT CATTGAAACC ACCTAATAAC 1140 CGTGATCCTC ATATCTGGAT CTGGTGCACA GAATTGACTG ATATATCTGT TTTTGTGATG 1200 AATTGCCTTC CGCAATTAAC TAGAAGCCCT AGAATGTCTT GGACCTTGCC TGGTCTTTTT 1260 TCCTTGTTTA TTTTGAAAAA GTAATACAGT AGTCCCCCCT TATCTGAGGG GGTGTGTTCT 1320 AAGACCCCAG TGGATGCCTG AAAGCTCAGA 1350
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