Tag | Content |
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EnhancerAtlas ID | HS133-13494 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:76330650-76331530 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr17:76331426-76331437 | GTTTTATTGGG | - | 6.62 |
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| Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
SE_02705 | chr17:76330662-76331532 | Astrocytes | SE_31461 | chr17:76330755-76331475 | Gastric | SE_34704 | chr17:76330482-76331438 | HeLa | SE_38941 | chr17:76330622-76331588 | IMR90 | SE_44143 | chr17:76330458-76331781 | NHDF-Ad | SE_44765 | chr17:76330515-76331617 | NHLF | SE_45620 | chr17:76329788-76335520 | Osteoblasts | SE_47352 | chr17:76329536-76331972 | Panc1 | SE_51835 | chr17:76330659-76331357 | Skeletal_Muscle_Myoblast | SE_55689 | chr17:76329782-76335716 | u87 | SE_58926 | chr17:76309354-76389031 | Ly3 | SE_61360 | chr17:76309626-76357699 | HBL1 | SE_62409 | chr17:76309367-76385525 | Tonsil | SE_63627 | chr17:76330640-76331454 | HSMM | SE_65603 | chr17:76330764-76331564 | Pancreatic_islets | SE_67525 | chr17:76329782-76335716 | u87 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I078333 | chr17 | 76329862 | 76331667 |
|
Enhancer Sequence | TAATTATGTC CTGTCATCTC CCTGCTTGTA GCTACTAAGA TCCCTTAGGA AAGATCCCAT 60 CCTGATTTAA GATTGCATCC CTAATACCTA TAACACAATA ACTTGCACTT ACGGACATGC 120 CATAGATATT TGTTGACTAA GGGCAAGAAT ATATGAATTT GTTTAGTGAT TCACTGCAGT 180 GTTTTGTGGG TGAGTAACAT AGTCGTGAGT TTCTAGTTTC CCCAGTCTAG TTTCTGGCCC 240 ACAGTGGCCT TGTTTGTCAT CTTTCTGTCC CTCTCCTCAT CTCAGGCCAA GGGTGAAAGC 300 CAGCAAGAGT CCGGGGCTGG CATCTACCCA GACAGCGTCT CACTCTGCTG CCCAGCCCAC 360 TTTCAAGTCA ATGTGGAGCT TCCCAGCTCG CCCTCCCCAT CCTGGATTTC AGATCCCTCC 420 TACCCTCACC CTACTTTCTC TCGGAGTTTG ACAGGGGAGC AGGTAGAACC TGGGGCAGAT 480 CTGCATTCCC CTGGGAGATG CTTCAAGCAG TGGCAGGGTC TTAGCCTCTG AGCTGCTCCC 540 TGGTAGGAAG GAAGCAACTG CCCCTGGTCT GTGTTGGGAG ATGGACAGAG CTTTAGGATG 600 GACAGGCGTT GGGGATGCAC CAGTACACAT AGGCGCTCAA TAACGGTGGT CTTTATTCTC 660 TTTCCTCTTC TGTCATCTGA CACGATTCGG TCTTCTCAGC TAAGGACTGG GTCTGTCCTT 720 CGCTCGTCCT TGTAGCCGTG ACTACAACCT TCCAAGCCAT TTTTGTTTTC TTAGAGGTTT 780 TATTGGGAGC TGAGGGTTAA TAGCACCCCA GCCCCTCCCA TCAGGCTCAA GGGGCTCTTT 840 TGCCTTCACT TGTGGTTGAG AGTCCTCCCT CCCTCCTGCC 880
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