| Tag | Content |
|---|
EnhancerAtlas ID | HS034-07599 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr12:113502370-113504120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr12:113502876-113502890 | GGGGCCCACTGGGG | + | 6.86 | | REST | MA0138.2 | chr12:113503825-113503846 | GCCAGTCCCCAGGACAGCTCC | + | 6.15 | | REST | MA0138.2 | chr12:113503207-113503228 | CCGAGTACCTTGGACAGCACC | + | 6.98 | | SPIB | MA0081.2 | chr12:113503471-113503483 | GATGCGGAAGTG | + | 6.74 | | TFAP2A | MA0003.3 | chr12:113503014-113503025 | AGCCTCAGGCA | + | 6.32 | | ZNF263 | MA0528.1 | chr12:113503319-113503340 | ACCCCTTTCTCCTCCTTCTTC | - | 6.25 | | ZNF263 | MA0528.1 | chr12:113503291-113503312 | GCCCTCTCCCTCTCCTTCTCC | - | 6.34 | | ZNF263 | MA0528.1 | chr12:113503316-113503337 | CTCACCCCTTTCTCCTCCTTC | - | 6.82 | | ZNF263 | MA0528.1 | chr12:113503346-113503367 | TCCTCCTCTCCAGCTTCCTCC | - | 6.82 | | ZNF263 | MA0528.1 | chr12:113503313-113503334 | CCCCTCACCCCTTTCTCCTCC | - | 7.17 | | ZNF263 | MA0528.1 | chr12:113503297-113503318 | TCCCTCTCCTTCTCCTCCCCT | - | 7.2 | | ZNF263 | MA0528.1 | chr12:113503334-113503355 | TTCTTCCCTCCCTCCTCCTCT | - | 7.61 | | ZNF263 | MA0528.1 | chr12:113503294-113503315 | CTCTCCCTCTCCTTCTCCTCC | - | 8 | | ZNF263 | MA0528.1 | chr12:113503331-113503352 | TCCTTCTTCCCTCCCTCCTCC | - | 9.13 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_11220 | chr12:113492132-113532554 | CD20 | | SE_25465 | chr12:113491507-113503091 | DND41 | | SE_58497 | chr12:113486066-113504185 | Ly1 | | SE_59675 | chr12:113485896-113536562 | Ly4 | | SE_60394 | chr12:113485972-113543650 | DHL6 | | SE_61231 | chr12:113486428-113542337 | HBL1 | | SE_61437 | chr12:113485785-113543165 | Toledo | | SE_62776 | chr12:113486575-113542506 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I113064 | chr12 | 113502643 | 113504041 |
|
Enhancer Sequence | TCATAAGGAC AACAGATACA GACCTAAAAC CCAGCTTGGC CCCTTGCTGG CTGTGTGACC 60
ATGGGCAAAT TCCTTAACGT CTCTGAGTTT ATTTCCTCCT CTGTAAAATG GGGATAAGAA 120
TAGTCCCTAG CTGGGAGGGT TGTCATGAGG ACATAATGAG ATACATAAAT GAGATATGTA 180
GATAAAAGCT TGGAGGATAC TACTTTGCAC GTAGTAAGCA CTCATGCTCG AGGAAGAAAA 240
AGATTTAAAT GCCTCACTAG GCAGATGCAC GGTGCCTTCA GCCATGGGAT GTGCATGGTG 300
TATGCCTGGA GCCTCTGAGA GGAGGACTTC CTGGAGGAGG AGTCCTTTGA GAGTGTGTGA 360
TTTGGGTAAA TAGAATGATA GGAGGAACAC TTACAGGTGG AGGAAACAGC AGGGGTCCTT 420
CAGCAGGGTC CTGGAGGAGG GTCTCAGGCC TGGGTGGCAG AGGGAGGCTG TGATGGGAGA 480
TAGGGGATGG GTAGAGGAGG CCTCGTGGGG CCCACTGGGG CCTGGCAGGC TGGGCTGCCA 540
GCTGCTGCCC TTTAGCAGCC AGGCCCCGGG GGACTCACAG CCACGCTGCA GGACCAGCCT 600
CATTAATCAC GGGCCCTTGG AGCTGGAGCA GGTGGGGCAG GGGCAGCCTC AGGCACTTCC 660
TACAGTCTGT CTGGGTTCCC TTCACCCAGC CAGCGGGTGT CACCCCATTT TACACATAGT 720
AAAGCTGAAG CTCAGAGGGT GGGGAGCCGC CTGCCGACGC TGAGAAGAGA CGGGTCTGAG 780
ATCAGATCCA GGTCTGCAGC TGGGTGCGCA CGGCCCTTCC CAGGCTCGCC CGGGCCACCG 840
AGTACCTTGG ACAGCACCAT CAACGACCCG CCCGCGCCTT CCGGGCTGGG GGTGGGGATG 900
CCCGGGACAG ACCCCCTCGC AGCCCTCTCC CTCTCCTTCT CCTCCCCTCA CCCCTTTCTC 960
CTCCTTCTTC CCTCCCTCCT CCTCTCCAGC TTCCTCCCAT CCCCCGCCTC ATTCTTCCAA 1020
AGGAGCTGCG GAGTCTGACC TGGAGAGGAA GGAGGAGATG GAAGCTGTGA TGGGAAGCGT 1080
GGGGGCTGGA GTAGGGGAGG TGATGCGGAA GTGACAGGTA GCGGGGCTGT GGAGGGGATG 1140
GTGAAGAAGG TGGTAAGGAG TGAAGCGTGA GGGGTTGGGA GGGGAGATGA TGGAGGGTGT 1200
GATGAGAGGG TGACGAGGAG GGGCCAGGAC GGGGAGGCCA CGGGGAGGCC AAGGGGTTGG 1260
GGCAGGACTG GTCACAGTGG CTCCAAGTGC CCATTCAGGC AGTAGGCAAT GGGGTTGAGG 1320
TCCCTAACTC TCTCTCCAGT GTGATGTTCT TGGTGCATGG GGGTGCCTGG GGTGCTCCCA 1380
GGCCTCCGCC CGCCACCTCT GTCTCTCCCT GGGCCTCCAT CCTTCCACCT GGCTCTGGAA 1440
TCACAACCGG TGGTAGCCAG TCCCCAGGAC AGCTCCAGTC CCTTAGATAG TCACCCCCAT 1500
GAGCCCACCC AGCCTCTGGG TTGACACAGA CACCCCCAGC AGCCCCTAGC TGCCTCTGGC 1560
TGACATCAAC TGAGGACATG GGGCCTGGAA CCTGGAAACA GCTACCTCGG GGAATGCTGT 1620
TGGTGAGGGC CAGGCTCTGG GTTCCCATCC CAGCTGCTTA CTAAGAATCA TGGGGTGTGT 1680
AGGCCGGGTG TGGTGGCTCA CATCTATAAT CCCAGCACTT TGGGAGGCTA AGGTGAGTGG 1740
ATCACCTGAG 1750
|
