| Tag | Content |
|---|
EnhancerAtlas ID | HS184-07634 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:52639720-52641960 |
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 | chr12:52641411-52641432 | ACCCCCACTCCCTGCTCCTTC | - | 6.16 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_02068 | chr12:52638893-52644556 | Aorta | | SE_33886 | chr12:52635925-52644054 | HCC1954 | | SE_36332 | chr12:52636699-52641658 | HMEC | | SE_47640 | chr12:52636838-52644749 | Pancreas | | SE_57989 | chr12:52640896-52641373 | VACO_9m | | SE_57989 | chr12:52641576-52642006 | VACO_9m | | SE_65936 | chr12:52636117-52644962 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 52640503 | 52640632 | | chr12 | 52640916 | 52641517 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I052242 | chr12 | 52635980 | 52644122 |
|
Enhancer Sequence | ACGATTGATT CCTTAGTCTC CAGAGGGGAA AGCTGTGGTT GAGTTTCATT AATTGAGGGA 60
ATAGGGCCAG AGTGCAGTCA GGGTGTGCTG ATTCCTGCTC CAAGGATCTT CCAGGACGCC 120
AGGCTGCTTC TCACTACAGA ACTAAGTGCT ACATCATGTG GGGCTAACTG ACTGTGGTGG 180
AGGGGGATCG TTTTGTTTGT CCCCAGAGAT ATTTGCAGAC TCACTTGCAG TCAGAGAGGA 240
GGCTGGAATG GGGGAGTCTG ATAGCACATT CTTCATGAAC CGCATGCCAC CTCTGTCTAT 300
GCAGCTGGGC CTTCATGGGC ATATTGTTGG GTTCGAACTC AACCTCTTCA TTCTTGGCTT 360
GTTATAAGAC ACCATGGCAA CAGAGAATAC GTAGGACATG TTTCTGCCCT CAGGGAGGTT 420
GCAGAGGGTG GAGGAGACAA AACATCCACA GAGGAAACCC CCAGAGACCA GTAACTTACA 480
TTTGTAAAAT GCTGAGTGTA TACAAGAACT TATTCTTTTC TGAGTATTAT TCCTAAGGGG 540
CCAGAGAGAG ACATGACGGA GGATGAATGG AGCAGCAGGG AAGGGAATGG GGAGTGAAGG 600
GGTGCTAGGG CCGAGGGCCT GGGTGCTGGG AGGAGAAGAG GAGACACAGG GCCGCAGGGT 660
ATGAGTAGGA GGCGGAGAGG AGGAGGAAGG GGCTTTGCCC CTGCTGCTGA CCCGCCTTCT 720
CCCTGGGTTA GCACCCAGTC TTCTTTGTGG GAAGAAGAAT TAACACCAAA AGTCTCTGGG 780
AACACAGAAG CTGATCTGGG CACAGGGAGC TCCAGCCAAG ATGCCTCTCT CTGCTTTCGC 840
CTCTCCCACA GGCACAGGGC CCCCAAATTC TCTACAACCC ATACCCTGGG CCTTCTGTTG 900
TCATAGAAGT CAGAGTTGGG GGACTCTTAG AGTGGTACCT GATCTGGCTT CCTCCCATGG 960
GAAGAAAAGG GGACTGAAGC TCAGAAATGG TCAGTAGTGT GCCCAAGGTC ACACAGCACG 1020
CAGAGACATC CTCTTCTGAA AGCTTAATCT CAGTCTGAGC TGCTGTAACC AGGCTTAGAT 1080
CCGGGTACTC TGAGAGGATA TGGTTCCCCC AACCCTGGGG GGATATGGAG GTAGATACCT 1140
TGCTTTTATC TCTTAACTTA TCAGAGTTGT GGTCCAGAAA CTCATTCAAA CTGGGAGGCC 1200
TACTTTAAGA ATACAAAGTT ACCAAAAAAA CCCCACTTAC TTAGAATGAG AAAAGTCACA 1260
CAGATCACTA GAGCCTTGGA CATTCAGGCC TCTTCCGTCT GAGTTCCTTA GGCATCGTAC 1320
CAGAAATTCT TCGAGTTGCT GCCTGACTGC AACCTGGCTC CCTCTCCCCA CCCACAAGTG 1380
CCAGCAACTC CCAGCACCAG CAGGGGCCAT TTAAGCAAGC CCCCTGGAAG CTTTCAGCAA 1440
ACCTCTCTCT TTCCCTCAGC CTTTGCTCTG CCTGCTTCCT GGGCTTGGGG CCGCAGAGGC 1500
CAGCGAGGCT CCCTTCATTC CCTCCACCAA AGCGAGGTCT TCCCTGCCCC CACAGAGCAA 1560
ACTGATCCCC AAGGCCAAGG CCTTGGTGAC AATGGGACTG TGAGTCACAA AACAAACATA 1620
GCCAGCTGTC CCGAATGGAT TTTTAATTTC TACTGCAAGA CCTGTTTCAG CCCCACTGGC 1680
TGCTTAAAGC CACCCCCACT CCCTGCTCCT TCCTTAGTCC TGGCTGGAGC CCCATTCAAT 1740
CAGTCAACGA TTCACGAATT ATTTTGACAT ATATTAAGCA ATGACTTCTC CAGGCCTCAT 1800
ACTGGGGATA AAAGTATCAA TAGGCCACAG ACACCTTTAG GATTTTATGA TACGGTGAGG 1860
AAAGGCAGCC ATCTACATAA ATAACACATA CAGCTACCAT TCACCGAATC CCAGGTGCTC 1920
AGGGCTTTAG ACAGATTATG TCATTTAACC CTCACAGGCC CATGAATTTG GTCCTGTAGT 1980
TGGGCCCAAG GCATAGGTGG GAAATGGAGG CCCTGAGACA TTGCCTGGGG TCAGGTGGCC 2040
AGTGGATAGA AGGGCCAAGG TGAACACTCC CTTCCTGCAT GCCTCCTCGC TCCTTTTACA 2100
AGGCTGAAGG CAGGCTGGAA GTGTGGGGCA AGAAGGAAAA ATCAATGATC CTGCTTGGGG 2160
CCTGGAAGGA GAGAGGGCTG AGAGCGCTTC CCTCCCACGC TAGGAAAGAG CCGTCCTCAC 2220
TGTCTGTCCT CTGCCCCCAG 2240
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