| Tag | Content |
|---|
EnhancerAtlas ID | HS069-08713 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr9:139524390-139526680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr9:139525101-139525122 | TGAGGAGGGGGCTGAGAAGGG | + | 6.01 | | ZNF263 | MA0528.1 | chr9:139524632-139524653 | TCTCCCCTTCCCCACTCCTCC | - | 7.03 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_24338 | chr9:139524405-139525154 | Colon_Crypt_2 | | SE_24688 | chr9:139520337-139525246 | Colon_Crypt_3 | | SE_25694 | chr9:139523633-139525332 | DND41 | | SE_33432 | chr9:139510552-139525295 | H2171 | | SE_67101 | chr9:139510552-139525295 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 4 | ID | Chromosome | Start | End |
| GH09I136635 | chr9 | 139524681 | 139524830 | | GH09I136630 | chr9 | 139524941 | 139525110 | | GH09I136634 | chr9 | 139525141 | 139525290 | | GH09I136631 | chr9 | 139525941 | 139526614 |
|
Enhancer Sequence | GTTGCAGGGG GGAGGGGAGG GGGGCGACGA CACCACCCTG TCCCCAGCTC CACTCCCTCA 60
GGCACCGTCT CCTCCTCACA GCCCCCACTG GTCTCCTTAC TGCGGTGCCC AAGACCCATC 120
CTGGACTGGG GTCTGGTGCT GGGAATCTCA CACTGGACCC CCAACCTGGC TCCCATGGGC 180
CTGTCCTGCC CAGCCCCAGG CTGCCCCTCA GCAGCTCTCA CCCCCTAGAC CCCAGACTCC 240
TGTCTCCCCT TCCCCACTCC TCCCAGGCTG GGCTGGGTCC CGCTGTGCCC ATGTCTGCCC 300
GCATATCTGT AGGACCACTC GCTGCCTCAC CCCTGCACCC CCACCTGCCG GCCACAGCCA 360
CTCCCAGCCT GCACCTGCCA GGGCTTCACA AATGACCAAG GGGAAATGAA AACACAACTC 420
TTCTGAGTTC AGCTGTCCAA GGCAGAGGCT GGGCAGTGCC CCCTGCCCAC CAGCTCCTGG 480
AGCTGAGCCA GGGGCTCTGG GAGTGGGGGA AGGAGTCAAA GACCCCCGAG CAGAGGAGAG 540
ACTGGAGAGG GACTGGTTGG GGTGAATCGG CCTCCAGCGT CTTCCAGCAA AGCGTCTCCT 600
CCCACCCACG CTGGCCTGCG ACCATTCCCC AGACACCTGG CGCCACCCAC CGGGCCAAGT 660
GGAGGCTGCG TGTGGGAGGG CTGTAGCCCT CAATGCCCTG GGGTGCTCAG ATGAGGAGGG 720
GGCTGAGAAG GGGAGGGGCC CTAGATGGGG AGGAACAGAG AAGCCCTGTT AGACGCATGC 780
CTTGAAGAAA CTTGGTTTAC ACACACACAC ATGCTTCCAT GTGCATGCAC ACACTGGCAG 840
ACACACGTAC ATACACACGC ACACATGCTC ACACAGATGC CCATGCTTGC ACACACCCAT 900
CCACGCTCAC TAATACACAT GCACGCATGC TCACAAACTG ATGCCCGCAT GCTCACGCAC 960
AAGCACACGT GCTCACACAC ACATACGCAT GCATGCTCAC ACACATATAC ACGTACATGC 1020
ATGCTCACAC GTGCACACAT ACACACGCAC CCATACTCAC ACACATACAT ACATGCCTGC 1080
ACACACACAC GCATGCTCAC ACAGACTACC GCATGCTCGC ACACGCACAC ATGCACACAT 1140
GCTCACATAC ATACACGCAT GCATGCTCAC ACATATACAC ACGCATGCAT GCTCACACAC 1200
ATGCTCGCAC ACATACATAC ACACATGCTT ACACACACAC GCACGCATGC TCACAGACTC 1260
CCGCATGCTC ACACACGTGC TAACACACGC ACGTGCTCAC ACATACACAT GCACAAATGA 1320
TCACACACAC ACCTGCATGC ATGATCACAC ATGCACACAT ATGCACCCAT GCTTGCACAC 1380
ATGCTGACAC ACATACGCAC GCAGGCATGG TCACACGCAT ACACACGCAC ACATGCTCTC 1440
TCACACACAC ACATACATGC ACACACATAC ATGCTCACAC ACACGCACAC ATACACACAC 1500
ACCCATGCTC GCACACACAC ACGCATGCTC ACACACGCAC ACACGCACCC ATGCTCACAC 1560
ACACACCACA CAAGCATGCT CCCACACATA CACACATACA TGCTCTCACA CACTCTATCA 1620
CACATACGAC TGTTCCTGGG GCTGTGCTGC CCTCCTGTGG CTGCTGACAA CTCCATGTCC 1680
AGCCCACTCA GCTGCCGGAT CCCCAGGAGG GCCACCATGG ATGTCTGGGG CCGAGGAGGC 1740
ACACAGCCAC CCGGGGCCAG GGAGCACCGA GGCCTGGGTA AGGGCAGAAG CCGCCAAGCC 1800
CCCGGTTTGC TCCACCCCTC AGTCCCCATC ACAGTCTGGG CCAGGACTCA GAGCCCTGGG 1860
TTCCCCAACG AACCTGCCCC TCCAGGGAAC CCAGGACCCC TTAGGACAGA GCTCCAGACC 1920
CCATCAAGGA CTAAAGGAAG AAAATTAAGC ACAAACAAGG TAGAAGAAAT AATGAAAACA 1980
CGAGTGGACA GAAATGAAGT AAAAAGTGGA CAAACAACAG AGAAAATCAA GGAAAGCAAG 2040
AGTGAGTGAT TCGGAAAGAT CCACAGAACC CACAGATTTC CAGCTGGACG AATCAAAGGA 2100
AACAAAAAGA AGAAACCACA AATCAGCACT GTCAGAAAGG AGAGGAGGCG CCATCTCACC 2160
TCCCACAGAC ACCGAGAGAG TGAGTGTCAG GAAGGAGAGG AGGTGTTGTC TCACCTCCCA 2220
CAGACACTGA CAGAGTGAAC GTGTCAGGAA GGAGAGGAGG CGCCGTCTCA CCTCCCACAG 2280
ACAGCAAGAG 2290
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