| Tag | Content |
|---|
EnhancerAtlas ID | HS156-10615 | Organism | Homo sapiens | Tissue/cell | P493-6 | Coordinate | chr7:2236300-2238700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr7:2237081-2237102 | GCCTCTCCTCACTCCTCCTCT | - | 6.21 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 2236417 | 2236530 | | chr7 | 2237309 | 2237392 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH07I002195 | chr7 | 2235308 | 2236399 |
| Enhancer Sequence | AGACACTGTG GTCACAAAGG AACAGGCATT CACCTGAAGA GGAAACAGAA AAACAGGGAG 60
AGTCTGGCCT TCAACACGAA CCCTCTTCAG AAGTCAGAAG GCCTCGGGCT CCCTGCTCAC 120
AGGAACAGTG CGGCTCAATT CTAACTCTCA CTACAACGCG GCTGACTCCA CGGCTCCTAC 180
TCCATGAGGC TCTCAACTGA CAACAGGAAA CACCGCCCAC CCTCCCCACA CTTCGGGGCT 240
GCTGAAACCT GCAGCGGGTC AGACAGCCCC AGGGACTTCC ACCAGCAGGG TCCTGCCAAG 300
GCGCCAGGTC CTCGCCCTGC GAATTCAGTG AGGAAAGAGG CCCCTTCACA ATTGGCGGAT 360
GTGCTCCTCC CTGATGAAGA CCTTCTGCGG CTCCTGTGAC CTGCAGGACG CGGTCCAAAC 420
CACCCTCAGG ACAGGACAGA TCCCTGCCAA CCTGTCCAGC TTCTGCCACA TCCCAGGAGA 480
ACTGTGGTTA GAACCAGCTG GAGCCACACA ACACTGTCCG AACACGCAGC ATCTGGCCAA 540
CCTGTGTGCT GCCAGCACCC ACCCTATCTG GAACATGCTG CCAGCCTCTC AAGTGTCATC 600
TCTTCAGGAG CCACGCTTGA CCTAGCAGAC ATATGCCCGG CTAGATCTGA GAGGACTGGA 660
AAACAGCCCC TGACTTATAG CTGTATCCCC AGCACCCAGC ACCAGGCCTG CACACCTATG 720
TGTTCAAGAA GCACTCACCA GTGAAGAAGA GGAAGAAACC CCACTGCTCT GGAGGCTTCT 780
AGCCTCTCCT CACTCCTCCT CTCATCTCCC GCCCCGACCC ACGCATCACT CCGCCGACGC 840
CTGGTACACA CGACGTGCAC TGCACAGCCA CCTTCTCCCT GCACACGGGC CCAAGCTCGG 900
ACACAGGCAC GACCAGGACT GGCGGGCTGC AGAGCTCTCT GACCCGGTGA GGCACTGGCC 960
CTCAGGCTCA AAGCCACCTG CAAACGCCAA AATCCCTCCA GACTCGGGCC AGCTGTCTGC 1020
TCCTCTGGCT CTGCCACTCC CCTAGGCCGG CTCATCCCTG CCCCTCACTG GGCAGGCCAG 1080
CCCTAGGGCT CCTCTAGGAG CCATGCAGGC CTGACATCGG CTGCTGTCTG ACACCTCCTT 1140
CTGGCTACAT CACTGACACT TCAAACACAC ATTCCCAAAA CAGAGTTCAC AACCCCTCCC 1200
TGCCTGAGAG CCAAAACTGG TCCTAGCCCC CGGGTCCCAG CCCCCAGGTC CCAGCCCCCA 1260
GGCCCCAGCC TGTGACTGAC CCCATCTCCC TGCACCCACA GGGCCCATCA GCCCCTCCTC 1320
TAAGAGCAGG CCTGGGAACA GGCCCAGGAC GGGGCAACCA CACCCAGTTC TGCCCCACAA 1380
GCGCCCCCGC TCATCCCAAG GTCCACCATG AGTTTGGGTT TTTTTTTTTT TTTTTGGAGG 1440
AAGGGTTATC TTTATATTTT TATTTTTAAA AATAGAGATA GGGTCTCACA GTGTTGCCCA 1500
GGCTGGTCTT GAACTCCCAG GCTCAAGCGA TCCTCCCACT TCAGGCTCCC AAAGTGCTGG 1560
GATTACAGGT GTGAGCCAAG GCACCCAGCC CAGCGTGGAT TTGTGCCAGG AAGAGCCAGC 1620
AGGAGCTGAC CAGCCCCATG GAAGCCTCCA GGCCGGCTGC CTGCTCTCAT CTCCCAAGAG 1680
CCCGCCTTTG CTTCTGCCAG CCACTCACGC TCTCCACAGG CTGCAGCCAG GTACACACCC 1740
CCCTTCAAGC AACAAAACCA CTGCCTGAGC ACCTGGCCTG CTCTAAGCCC AGGGCTGAGA 1800
CAAGGGGGAG CCAGCCACAC ACAACACCAG GAGCGCTGGC ATCGCCGGAG CAAGGAGCCC 1860
GTGATGGCCG TCCACCCGGG ACAGCAATCG CGCTCTGCGG CACGAGGCTT TCAACAGAGG 1920
CGAGTGCTTC CTGGGGGTCA AGAGCATGGA ACACACACTT CAGGCCCCCT CTCCAGGCTG 1980
CAGGCCAACA GGCGTCCATG AGACAGACAC TCCCTGATGT GTCCCACTCA GTTCTCCTGC 2040
CGCTGAGTGA CTCTCCCAGG GAGGCCCAGA GCCACATGCT CTTGGTAGCC CCTACTCCTC 2100
CAGGTGTTAA AGCAGGTGCC CATGTACAGT CCACAAGCAC AGGCCATCAG GCTGGGCAAG 2160
GATGGGCAAG GAACCAGGCC CCTGCCCTTT GAGGCTCAGG AGCTCCAAGC TACAGAATAG 2220
GGTTCCAAAG CTCCAGCCAC TCGGAGGACA CACAGGCCAC AGGAAGCCGG CGACCAGTCC 2280
ACAGAGAGAC GCGCTGTGGG GCCCGACAGG CTGAGGTCAG GCAGTGGGAT CCCCCCTTCA 2340
CAGTCCTCCC GGCCTTGGGC GGGGCTATCC AGGAGGGGGC TGCCCCTCCC TGCCAGAGTG 2400
|
| |
|
|
|
