Tag | Content |
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EnhancerAtlas ID | HS164-10709 |
Organism | Homo sapiens |
Tissue/cell | Raji |
Coordinate | chr6:34868290-34869630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr6:34868758-34868771 | TTCTAGAAAATTC | + | 6.34 | ZNF410 | MA0752.1 | chr6:34869140-34869157 | TAGGATTATGGGATGGG | - | 6.65 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29278 | chr6:34865444-34870148 | Fetal_Intestine_Large |
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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 |
GH06I034897 | chr6 | 34865445 | 34870148 |
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Enhancer Sequence | TTCTGGAGCT CAAGCGATCC TCCTGCTTCA GCCTCCCAGA GTGTTAGAAT TACAAGCATG 60 AGCCACCACA CCTGGCCATA ACAACTGTTT GAGGAATACA CTAGTAGTAT TGCCATTTTA 120 CTGGTGAGGA AACTGAAACA CAGAGAGATG AAGTAACTTG CCAAGGTGCA GTAAGCTAGT 180 AAAAGTTAGA GCTTAGTTTT GAACCCAGGC AGACAGGCCC CAGAGTCTTT GCTCTTGGTT 240 ATTATGCAAC TGGGACTTCT TCCTTTTACC CAAGAATGTA ACACAAAGTC CTTTGGGAAG 300 ACTTTGACTA CATACAGTGA GGTAGGCTCA TTAAAAAAAA AAATTGGCAA ATTCCCTGGA 360 ACACAGGAAA GTTAGATAAA GAGAATGCCT TTACGTCTAT GCCAAATAAT ATATTAGTTT 420 AGAGAATGTG GGGGACTTCC CTATAGCTCC CACATTGCTT TTTCGGACTT CTAGAAAATT 480 CTCATCTCAT GTAGGTGCAC GTGTTCATGA ATTTTACCTG TGAGAAAATT TAAGTGGTCC 540 CTGTGCCCCC CGCAACCAGT TCAAAATGAT AAAAATTAGT TTTGGACCCA TAAGCTACAT 600 AAACTGCCAG ATGCACTACC AGGGCCAAAG TTTGTACAGG GGAAGTGAAT CTAAACAATT 660 GGCAAGAACC AAAAGCCTGT GTATTTGAAG TTATTTCCAA CTCTGTTTTT TTTTTTTTTA 720 AACAATTCGC TCCCTCATTA GTGATTAACA ACCAAAATTT GCATTCTCAA ATAATTAGTT 780 GGCCCATAAA ATGTTTTTCA GACAGTATTA TCTGGCTGGT TCAAATGATG GTTGATGCTG 840 TCTTGAAGCC TAGGATTATG GGATGGGAAA TGTTACTTTC CATAATCCTT GGTACTTTAA 900 TCTTCACAAT CCTTCAATAC AGGTATTAGT GCCCATTTTA CTGATGATTT TCTAGTGGTT 960 AAATGACTGG CTTAGAACTG GGCTGAGGTG GGGTTTTTTT TGTTGTTTCT TTTCTGAGAT 1020 GAGGTCTCAC CCTGTCACTC AGGCTGGAGC ACAGTGATGC AATCACAGCT CATTGTAACT 1080 TCAGCCTCCT GGGCTCAAGC AATCTTCCCA CCTGAGTCTA CTGAGTAGCT GGGACTACAG 1140 GCTCATGACA CCATGCCCGG TTAATTTTTG TATTTTTTGT AGAGACGGAG TCTTGCCATG 1200 TTTCCCAGGC TGGTCTTGAA TTCCTGGGCT TAAGAGATCT GCCCACCTTG GCCTCCCAAA 1260 GTGTTGGGAT TACAGGCGTG AGCCATCACA CCCAGACAGG ACTGAGGTGT TCTGTTTGTG 1320 AGGCCTTTAA GGGTCCTATT 1340
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