Tag | Content |
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EnhancerAtlas ID | HS026-02844 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr1:204553510-204554910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:204554858-204554879 | CTATTCTTCTGCTCCTCCTCC | - | 6.18 | ZNF263 | MA0528.1 | chr1:204554784-204554805 | GTCTTTCCTTCTCCCTCCTCC | - | 6.41 | ZNF263 | MA0528.1 | chr1:204554823-204554844 | TTCCTTTCCTTTCCCTCCTCT | - | 6.58 | ZNF263 | MA0528.1 | chr1:204554861-204554882 | TTCTTCTGCTCCTCCTCCCTC | - | 6.95 |
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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 |
GH01I204584 | chr1 | 204553659 | 204554565 |
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Enhancer Sequence | TCACTCAGTG GTTGCTCTGC TTGTTTATAT CACAATGTGG CAGGCACTGG GCCAGGTGCC 60 AGGCACTGAG AGATGAATAG AATGTAACCA GCCCTTAGGA CACTTATGAT TTACCAGAGG 120 AGATGGCACA AAAAGCATAT TAAAAAGCAA TGTGGCAAAT TAAATGGTAG TAATCCTACC 180 AAGTGATAGT GCTCCTGGGA TTGGGTTCCT CTCAGATGCT CCCCAGGGGC TACTGGAGTG 240 ATGTCAGGTA AGGCAGGACA CCAGGAAACA CCCATTCTCC CGGGCTCTCT GCAGAGCAGG 300 CAGCTTTTGG ACCTACCCGC TTCAAGGAGC TGAAGAAATG CCTTCCTCCT CACCTCTCAG 360 GCTCACAGGG AACATTTTTC AAAGGGAAAA ACTCTTTTTT TTTTTTTTTT TGTAGTCATC 420 CAATGTTTTC AACCCTAGGG CAATGGTTAG GGAGAGAGGA CATCTTGTGG GTGGCCTATA 480 ACACGGTCAG TAACCTTATG CCACAAAGAC TACACATGAC ATAGAAAGGT ACTTATGTTG 540 TGCACCGAGG AGGCACTGAC CCTGTGCATT CCCAGCACCT CAGAACCGCT AGCTCTGTGC 600 AAACCTTCCA GCCACCTCGG GCCCAGGAAG GCGGGGTGGG GGCCTTGATT CAGAAAAGGC 660 AGAGACACTG CAGTCCTGGG GAGGGGTGAT GTCTAGAGCC TGAGAGGAGC AGTGGAGCAC 720 TCACGGGAAA TGCAAAGCAG ACGCAAGACC AGGCCCAGAG CCTGGCGGAA GTGGGGAGGG 780 GTGGGGCAGG TGTGGGGCAT TAGTTGGGGA GGGGCTTGCT AGGAGGAGGT GACTTCAGAA 840 GGCATCTGCG GACTGTGGTC TGGGACTCTG CTGGATGTGG CATGGCTTTG CCACCCTCAA 900 CTCTGGTGTG TTAAAGAGGT AAAGGTCACA CGTACACATG GATGAGGACA GGGAAGACAC 960 ACAGGAAACA AAAACAGATT TGTTAGGGCT GTCGAAGAGT GGTTTGCTTA TTTTGAGGCC 1020 TCTCCCCATT TCTCTTTTCC TTATCAGGAT GTGTACGGCA CCCGCATCCC CTCCATCTGC 1080 ACCCGCAGCC ACAGCCACAG CCACAGCCAG CGCTATGTCC CGTTGCCATT CACATTCATA 1140 CCTGCAACGT ACACTCATAC ATGTGTCGGA TATTTGCGAA GAAGCTCCCT TTCCCACCTA 1200 GGTAAATGCT AGCTTCCAGA AATTTGAAAA AAAATGAGTG TAATTCCTAC TGGGTTGGTT 1260 CCCAGCAGGC CTTTGTCTTT CCTTCTCCCT CCTCCAGGCC CCTCTTCTTT CCTTTCCTTT 1320 CCTTTCCCTC CTCTACCTCT TTCCCTTCCT ATTCTTCTGC TCCTCCTCCC TCCCAGCTGG 1380 TTCCCTATTT CCCTTACCCC 1400
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