Tag | Content |
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EnhancerAtlas ID | HS042-20032 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr17:71375690-71377030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr17:71375692-71375713 | GGGGGAGAGTGGGGGAGGGGA | + | 6.46 | Zfx | MA0146.2 | chr17:71376989-71377003 | GAGGCCTGGGCCCG | - | 6.41 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_69033 | chr17:71375046-71375917 | H9 |
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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 |
GH17I073378 | chr17 | 71375047 | 71375917 |
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Enhancer Sequence | GTGGGGGAGA GTGGGGGAGG GGAAGCACAC TGAGGTCACC GTCATTGCTG GGAAGGTGTC 60 CCCAGGGAGG GTGGAGGCTG CAGGGGGAGG AATGAGGCAC CCCCGCCATT CTAGCCCCCT 120 CTGTGAAGGT GCATGAAGGA GGAGGTGAGA GGCGGGGCCC CCAGGGGACG CTCTGTGCCA 180 ATCTGGACAT AGGGCAATGC TGGTTGGCCT CTTGGCCTAG GGTGGCCGTA CATTTTATTG 240 TTCAACTGGA CACTTTTGAG ACTGAAACCA CTATGAATAT TTACACCGGG ACAACCAGTG 300 TAAACCAAAG CTGTCCTGGG CATGCCTGGA CATAGGGTCA CCCCCTACCC CCAGCCTGTC 360 CTCTTTCCCC ACCGTGACAG ATGCCCAGAG TCCCCATCCA CCAACTCTTT ACACAGCGGG 420 GCTCAGCTCC AGGGGGGAGG GGCGCATTGG ATGTGAATTC TGGACTAAGA AACCTGATGT 480 TTCTGCCAAG TTTGAGGTGC TTGGCTGAGA ATGCCTGGCA GAACTTGGGA ATGGGACGCA 540 GCTGCAAGAA ACGGGCGCAG TCACTGTCCC CCGTAGCTGA AAGTTTCTCC CACCCTCTCC 600 ACTCTTCTCT CTGGGTTCCC TGCCCCTGCT TCCTTCCCCT GGGTAGGTCT ACCCTTTAAC 660 AGGGTTGTGA GAGGGGTGTC ACCCTTGCCT AGCTGTCTAT GCAGCCTGGG TTGGTCATTG 720 GTTGACGGAG GAAGGAGGAA GAGAATTTAG CCTTAAACTA GTGCTATTTT CTCCTGAGCA 780 CGAAACCCTC TTGCCTAAGG CCCTGGGTTT CAGGAAGAAC CACGGCTGAT GCTTTAGAGA 840 AAGATCAAGG GTTGGGGCAT GCAAGCAGCA GGAACATGTC TGGTGCACGG GAGGACGACG 900 GACGCAGGTG ACTAAAACTG CTGTCACCTC CCTCCAGGTG TGGGGCCAGA CTGTAAGACC 960 CAGCTGGGCC GAGAAGTGCC TTCGATGGGA CTAGATGGGG CAGCAACCAC GTGGACACCT 1020 GCCCACCTAC CCAGCAGCGT CCAACAGCTT CTGCTGCGGC CCCGCTGTCA CTGTCCCCCG 1080 ACCCAGCCGA GCACAGGGTT ACAGACTTCC CTTTTCCAGC CCACACCCAA CAGAGGGCAG 1140 GCTTGAAGGA GACTTTCCCT GTCATCGGCC TACTTTTCCG TGTGTTTAGG GTTATCACTT 1200 GTGTTCAGGG TAGTCCCGTT TCTTAAGCCC CCTGGGGTGG GCACACCCCC TCAACCTGTG 1260 ATCAGGTCTC TCAAGGAGGC CCCACTCCCA ATCCCCTGCG AGGCCTGGGC CCGCGATGAA 1320 GCCACCATGC AAGGAGACTT 1340
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