| Tag | Content |
|---|
EnhancerAtlas ID | HS141-06533 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr15:75943470-75944560 |
Target genes | | Number: 16 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr15:75944335-75944356 | CCTTTCTTTCTGTTTTTTTTT | + | 6.31 | | JUN(var.2) | MA0489.1 | chr15:75943843-75943857 | GGGAAATGACTCAT | + | 6.92 | | ZNF263 | MA0528.1 | chr15:75944372-75944393 | TACCTTTCTTCCTCCTCCTCT | - | 6.25 | | ZNF263 | MA0528.1 | chr15:75944369-75944390 | CTCTACCTTTCTTCCTCCTCC | - | 6.86 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_00448 | chr15:75938236-75946236 | Adipose_Nuclei | | SE_01620 | chr15:75938135-75947935 | Aorta | | SE_15343 | chr15:75942263-75945629 | CD4_Memory_Primary_7pool | | SE_24007 | chr15:75943606-75944336 | Colon_Crypt_2 | | SE_24007 | chr15:75944364-75944964 | Colon_Crypt_2 | | SE_25223 | chr15:75943483-75945030 | Colon_Crypt_3 | | SE_26310 | chr15:75943073-75945045 | Duodenum_Smooth_Muscle | | SE_26676 | chr15:75938183-75946271 | Esophagus | | SE_31932 | chr15:75943442-75944962 | Gastric | | SE_34597 | chr15:75943251-75944741 | HCT-116 | | SE_36093 | chr15:75943958-75944842 | HMEC | | SE_41356 | chr15:75943214-75945219 | Left_Ventricle | | SE_42347 | chr15:75938366-75946340 | Lung | | SE_44203 | chr15:75938363-75945159 | NHDF-Ad | | SE_44859 | chr15:75943294-75944772 | NHLF | | SE_45931 | chr15:75943206-75944509 | Osteoblasts | | SE_47752 | chr15:75943477-75944326 | Pancreas | | SE_48850 | chr15:75943188-75945007 | Right_Atrium | | SE_50411 | chr15:75938538-75945376 | Sigmoid_Colon | | SE_52931 | chr15:75943160-75944756 | Small_Intestine | | SE_53820 | chr15:75943206-75945378 | Spleen | | SE_56214 | chr15:75943156-75945188 | u87 | | SE_64409 | chr15:75943006-75943839 | NHEK | | SE_65676 | chr15:75943323-75946340 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CACAGACCCA ACCCAGATAA CAAGAGCTCA GAGTGGGGGC CTGTCTTGTG CTCCTTGCAA 60
GTTAACCTCC CCACCTTTGC AGCTTTGGAA GCTACTCTCA CCACTGTGTA TTCTCTTTAT 120
GAGCGTCTTG TCTGTGTGCA GGAAGATCCC TGTCCCCATT TTGCAGATGA AGGAGCTAGT 180
GTCCACAGAA GAGTGGTTGC ACAGCCTGTG GCCCGGCTGG GACTGTCCCT TCCTCCTGCC 240
ACCTCCCCAA GGACACGTCC ATGTTGGCCA CTTCCCAAGC CTAGCCATGT TTTCAGTTCT 300
CATGACCCCC TCTGTGGGGG AGGGACAGGA TGGGCCTCTG CCTGTTACTG CTGGGGCTGT 360
CCATGAACTG CCGGGGAAAT GACTCATCCT GGGTCACACA GGGGCACTCT GGCTGGGCCA 420
GGGGTGCAGA ATCAGGGGTC CAGGGCACTG TCCACATGGC CTATCCAACT CCTGCTTCCC 480
AAGCCTGGCT TCTCTTCTTG CCTGAGGAGA GAGCCAGTGG CTGCCCCAGC AGGTGCCTGA 540
GTCCTGGGCA CAGCTGGGAG GGCAGATGTC AGGAGAGAGG TGTGATCCTC CCTGGGGCTG 600
CTTGGTAACT CGTCTGCAGG GCGTGGAGCT GGCTCCCTGG CCCTTGGGCC CTGAGGTTAG 660
ACCTGGCTTG GTGGGGAGTT TGACTCTGGG TGGGGCCAGG GGGCAGACCT CTGCACTGAG 720
CCTGGGGAAC AGGAAACATG TCACCCACCA CCACCAGGGA GGGCCTGGGG TAAGCTGGCC 780
TTGCTTTCCT TTACCAAGAG GTTGACTTCT ATAACTTCTC CAGCTCCCAG CCTCCTTTCT 840
CCCCTTGCTA TATCCTCTTC CTCTTCCTTT CTTTCTGTTT TTTTTTTTTT TTCTCTCATC 900
TCTACCTTTC TTCCTCCTCC TCTGAACTCC AGGAAACACA AACCTGAGTG CTAGTCTTGG 960
CTCTGCCCCT AGATTGCTGT GCGTCCCCGG GGAGTGCCTT TGCCCCTCTG GGCCTTAGTT 1020
TCCTGATCTG TAAAACAAGG GAATGGGGTC CCAGTGAGCC ATCAGGCCTT CAAGGGAGTG 1080
GGTGGGAAGG 1090
|
