| Tag | Content |
|---|
EnhancerAtlas ID | HS024-05800 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr16:24620590-24623500 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr16:24622060-24622081 | CTCTCTCTATCTTACTCCTCC | - | 6 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH16I024609 | chr16 | 24621122 | 24621330 | | GH16I024610 | chr16 | 24621481 | 24622121 |
|
Enhancer Sequence | GCCTCAGCCT CTCAAGTAGC TGCGATTACA GGTGTGTGCC ACCATGCCCA GCTAATTTTT 60
TATATTTTTA GTAGAGATGG GGTTTCACCA TGTTGGCCAG GCTGGTCTTA GAACTCCTGA 120
CCTCAGGTGA TCCACTCACC TTGGCCTCCC AAAATGCTGG GATTACAGGT GTAAGCCACT 180
GCACCCCGCC AAACCCAGCT GATTTTTCAG TCGATTTAAC TGTATCCTCA TTAAGGGAAG 240
AAATGGAGAG ATGTACATAT GTATGAGAGA GAGAGACAGA GAGAGAGAGA GAGAGAGACA 300
GAGAGAGAGA GAGACAGAGA GAGAGAGAGA GAGAGAGACA GAAGGGAAAT ATCTGCAGAG 360
AGAACAGAGC TATGATCACT AAGTAGAACA GAGGCAGCCT AATCGCCTAA TCAGATACCC 420
AGTCGGGGCC CCACCTGACT CCTACTGCAG CTGGGGGGTG GAGGGACTAG AAGGTTCAGC 480
TGGAGTGGTC TCCCCTTCTG CAGCTCCAGT CTCCCCACCT CCAACCCCCA CTGCCACTGC 540
CCCGTGAGGA GGCTTGGAAG CTGTGGGGAG GGGAGGCAGC CGAGTTGGGC TTCTAGAACG 600
AGGCGGGATG GTGTGAGCTC AAACGCCCTG CAATTGCTGG AGCAACAGCG GCGACACTTG 660
AGTTATTCAC AAAGGCTGGA ATTCAAATGA GGCTGGCACC GCTCCAAGTC GCAATAGCTT 720
AGGAGGAGAG AGAAAGGCAT ATTAACTATT CATCAAGGTC TTCGCGTTGC ATGGGCTCTG 780
AGGGTTCTCC ATCTGCGTCC CTCCCTCTGT CACTGACTGG GGGTAGGGGG CGGGGGGTCC 840
CCCAGAAGCA CTTTATCTGT CAGTCTGTGA GCGGGGGCTG GGGGTGGGGG ACTGAAGTTA 900
GGCAGATTTG TCTCATCACA TGATGGGGGA CCTGTATCAT GTGATGGCTC CGGTGATGTT 960
GGAGGCGGCA TGTGACTCCC AGGGCTACGT GGGTTCAAAA ACAATTTAAT ACAAAAACAC 1020
AAGCAGGTTC CCCTCCTCTC CTTTGCCTTT GGTCTGGCTC TCCCCATCGC TGGGTTCAGT 1080
GCCTGACTGA ATGGAAAACC CGTCGTCTTG CAGCCACTAA CCTGTGAGCG CCGGGTACCT 1140
GGAGACCAGG CCCCTCTGCT GGGGGCCCCC AGGAGCGGTG CCCCATCATT TTGCAGCCCA 1200
CTGACTCCCA GCCTGGTAAG TTACTGCACA CTTTCAGCAA TTATCTGCGA AGCTTTCCTC 1260
AACTGCCTCA TTAGCATGCG CAGGGCACCC TCGCTGGGCC CGTTGGAAGG GAAGTGCCTG 1320
CCGGCTCTGG GGAGCTGCGG CTCTCGGGCC CTGCCAAACA GACGCAGCCT TCCTAAGGAG 1380
CAGCGCTGCG CTGGCTCTGC TGGGGTGGAA GGAGCTTCTC CTTCGCTGTC CTCCCTCTCC 1440
CTTCCCAGCC CATCTTATTC CGAGCCTCTC CTCTCTCTAT CTTACTCCTC CTAACCTCTC 1500
TCACCTCTCA CCTTCCCCCT TTCCACCCCC TGCCCTCAGA TTTATTTATT TATTTATTTA 1560
TGACAGAATC TCGCTCCGTC GCCCAGGCTG GAGTGCAGTG GCGCAATCTC GGCTCGCTGC 1620
AACCTCTGCC TTCCGGGTTC AAGCGATTCT CCTGTCTCAG CCTCCCGAAT AGCTGGGATT 1680
AGAGGCGCCC ACCGCCACAC CCGTCTAATT TTTTTGTATT TTTAGTAGAG ATGGGGTTTC 1740
ACCATGTTGG CCAGGCTGGT TTCGAACTCC TGACCTCCGG TGATCTCCCC GCCTTGGCCT 1800
CCGAAAGAGC TGGGATTACA GGCATCAACC CCTGAGTCCA GCTGGATTTT CTTTTTTATT 1860
CACATACCTT TCTGTCTCCC ACTGATTTTT CTTAGGAGTT CCTCTCATCC TCTAACCTCG 1920
CTTTTTAAAA TTATTTTTCT GGATACCTAG ATTTTTGTCC TTTCTGGCCA GAGCCTGAAA 1980
GAACAGCTTC TAAGGACTTG GTGATTGGAA ATGTACCTTC TAAAAAAAAT TCTTTTTTCA 2040
CTAAGACAGT GTAGAATGCC CAGTTCCCGC TGTGTGTACG TGCGTGCACA TATGTGTTAA 2100
AGGAGATGGA TACATTGCTT GGGGCCATCA GAACTGTTTC CTGGGAGGTG GTTTCTTGGC 2160
TCCACACCCC AGCTCAGCAA GGGAATGATC AAGTGATAGG AGGCACAGTT ACAGCAGTCA 2220
GGAGACAAGG CACTCGGACC CCAAACGTCT GACTCTCTGT GGGAGAAACC AGGGCTCAAA 2280
GCAGGAGCAA AAAATCTAGT GCTGGATGCG CTCGGGCATC GAGAGGCATC TCGTAGAGCT 2340
GGCTCCGAGT TTGAGGCCAC ACCTTTGCAG AATGAGGCAG CATGTGAGCG ATTTAGTTCA 2400
ATGTAATTGC AGTGGAGATG GACAGGGAGA GGACAGATTA GAATGATGTT TAAGGGATAG 2460
AAATAACAAG TCTTGCAGAT ATATTACATA TATTAGTTGA ACCATGGGGA AGCCAAATGT 2520
GAATTGTGAA ATTATGGCAG TGGCTGGACA CAGTGGCTCA CACCTGTAAT CCCAGCACTT 2580
TGGGAGGCTG AGGCAGGCAG ATCACCTGAG GTCAGGAGTT CGAGACCAGC CTGGCCAACA 2640
TAGAGAAAAC CCCATCTCTA CTAAAAATAC AAACAGTAGC CAAGCATCGT GGTGCACATC 2700
TGTAATCCCA GCTACTCGAG AGGCTGAGGC ACGAGAATCG CTTGAGCCCA GGAGGCAGAA 2760
GTTGCAGTGA GCCGAGATCA TGCCACTTAA CTCCAGCCTG GACAACAGAT CAAGACTCCA 2820
TCTCAATAAA ATAAAATGAA ATAAAATAAA GTAAAGTAAA ATTAAATTAA ATCATGGCAG 2880
TATCTGTAGC CCCAGAGAAA GGAGATGGTG 2910
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