Tag | Content |
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EnhancerAtlas ID | HS176-35437 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr6:127686960-127688130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr6:127687964-127687980 | TGTTGCCATGGCAATG | + | 6.14 | RFX1 | MA0509.2 | chr6:127687964-127687980 | TGTTGCCATGGCAATG | - | 6.17 | RFX2 | MA0600.2 | chr6:127687964-127687980 | TGTTGCCATGGCAATG | - | 6.66 | RFX2 | MA0600.2 | chr6:127687964-127687980 | TGTTGCCATGGCAATG | + | 6.67 | RFX5 | MA0510.2 | chr6:127687964-127687980 | TGTTGCCATGGCAATG | + | 6.92 | RFX5 | MA0510.2 | chr6:127687964-127687980 | TGTTGCCATGGCAATG | - | 7 | ZNF263 | MA0528.1 | chr6:127687053-127687074 | TGGGGAGGAGAAGAGAGGAGA | + | 6.19 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09484 | chr6:127686832-127688020 | CD14 |
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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 |
GH06I127365 | chr6 | 127686618 | 127689100 |
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Enhancer Sequence | AAGGATATGC TTCAGAGCAT CTAAACCGTG GGTAACTTTT AACTGACCAC TTAGCCAAAG 60 GCTTTCATTT CCTAGCTTAC CTAATATTAT GGTTGGGGAG GAGAAGAGAG GAGACATTCA 120 CCCGTTGCAC CAACTAATCT CCCACGCAGG ACTTGGGTAT AGGTCTCTCC AGGTTCCCCC 180 AGCTTGAGTG GGCTCAGCTG CCATATTGTG AGAGGGACAG CACAGGGACC TGTAATCCAC 240 TGACCTGCTT GGTTGGAGCA GTGGGTCCCA CACAAGGCAG CAGCACCATG GCCACTTGAT 300 CCTCCACTTT GCTCTGCTGC CTGCCGGGGA AAGATGATGG CTCTTAAAAG AGTCTTTGGT 360 TAGTGTTATA GCTCTGTAGT GTTAGAAGCT ATTTATTGTT ACAGCCTCGG TGTTACAGCT 420 CTTGCAGCCT CGAGATCAGA CATTTTTGCT GTCTCTCTCC TTGTGGTATT GCAGATTGCC 480 ATGTTTCCCT CTCACCAACT ACTGTCTCTT GTTATTTCAG TCTCTCTGAC TGCCATCTTT 540 CATTGTCTGT CTCCAGTCGC TGCCTCTCTG TCTGTACTGT CTCACCATCC AGGTCTCACT 600 GTCTCCACCA ATCGATCACT GCCATTTCCA CCAATCACTG CCGTCTCCAC TGTCTTCCTC 660 CCTTCGCTGG TCACCAGATG ATGCAAGACA GGCAAGCCCC AAAATTCAGT CTTAGCCCGG 720 GAGGGTTCTT GGCTTAGCCC AGGAAATAAT TCAAGGGTGA GTCAGTGGTA TTAAACAGCA 780 ACTTTTATTA AAGTGGCAGC ATACAGCAGC AGCAGAAGTA CTGCTCCTTG CAGAGCAGGG 840 CTACTCCATA CTCCCAGAAT AACAGCTCAG AGGCAGTTTT GCAGTCATAT TTATACCCAC 900 TGTTAATTAT ATTAAAATTA AGGGGTGGTT TATGCAGAAA TTTATACCAT GAGAGAGGTA 960 ACTTCTGGGT TGTCAGGTCA TTGCTATGGA AAGGAATGTT AACTTGTTGC CATGGCAATG 1020 GTAAACTGAC ATGGCACATT AGTGGGCATG TCTTATGGGG AGGTGCTTCT GCCCCAGACC 1080 TGTTTTAGCT AGTACTCAAT TTGGTCCAAT GTCTGAGCCC TGTGTTGAGT CCTGCCTCCT 1140 AGCTCATTTT TAAGGTTCAT TTAAGCCATA 1170
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