| Tag | Content |
|---|
EnhancerAtlas ID | HS077-00762 |
Organism | Homo sapiens |
Tissue/cell | H128 |
Coordinate | chr1:150770180-150771540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:150771266-150771287 | CCCTCTCTCTCTTGCTCCCTC | - | 6.47 | | ZNF263 | MA0528.1 | chr1:150771263-150771284 | CCTCCCTCTCTCTCTTGCTCC | - | 6.57 | | ZNF263 | MA0528.1 | chr1:150770186-150770207 | TCCCCCACTCTCCCCTTCTCC | - | 6.64 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09956 | chr1:150765301-150770958 | CD14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 150771037 | 150771189 | | chr1 | 150771200 | 150771400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I150792 | chr1 | 150765302 | 150770958 |
|
Enhancer Sequence | GTACCCTCCC CCACTCTCCC CTTCTCCAGG GGCCCCCAGT GTTCCTGATC CTGCCCGGGT 60
GTGTCCTTTC TTCCTCCCAG CTCTCTTGGA AGCTATCTCC ACACATGGTA CCTGATCATG 120
AAAGAACAGG GTAAGTGCTT GGACCTGGGA GTCAAGAGAA GGGACAACAC AGGACAGAAG 180
CTGTGGGAGA CTTGGGAAGA TGCTCAGGTT CACCTTGAGT TGGAACTGTG ATATAAAAAG 240
TTGCTTCAGG TTTGAACAAC ACCACTGCGT GAGTCTGTCA GCGACCCAGA GTCTAGGGCT 300
CCTGCTCCTT GGAGGGCACT AAGGACAGGA GATTTAGCCA GTGCTGCTGC CAGGTTAATG 360
GTGATCAGCC AGGAAAGGAA AACTATAATT GTTATCAATC TGCCCCTCCC CAAAAGTCAC 420
AAGGTGCTAA AGAGAAATGG GAAGCAAGGT ACCCTGGAGT TTTCTTTGTT CCCCAACATA 480
GGAAAGTAAA CACTAACTTT TTTTGTTTAT ATCTTATTTC TAAAAAATGT TTCTCTTCAC 540
AATCTTTGGC AAGTTCTTAT ATACGTGTAT CTTAAGTGTA TTTTGAAGGA AAAAAACTGT 600
TCAAAGGAAT ATTAAACCTT TACGCTGTTC CCCTACTGTT AAAGACAGAT TGCTAATGGA 660
AACCATCTAA GAAACTGATC ACATTAGAGA CAAAAGAAAG TAAAAATACG TAATTCCAAA 720
GCTCCTGCTG GTTCTTTGTA CTGCTTTATC TCATGGTTAG TTAGGTCTGT CTTATTGGGC 780
TCTGAGCTCA CTGAAGGTGT CATCTGCTCG TTGGTTTATG TATGTCACTA AGCACCTTGC 840
ACACAGGGAG CATCTGCCCA GCACATAATT GAGCACTATT GTCTGGCGGA TATGGTTTGG 900
ATGTGTGTCC CCTCCCAGTC TCATGCTGAA ATGTGATCCC CAATGTGGGA GGTGGGGCAT 960
AGTGGGAGGT GTTTGGGTTA TGAGAGTGGA TTCCTCATGA ATGGCTTGGT GCCATCGCCT 1020
TGGTGATGAG TGAGTTCTCA CTCTATTAGT TCATGCAAGA GCTGGTTCTT TAAAGAGTCG 1080
GCACCTCCCT CTCTCTCTTG CTCCCTCTCT CACTATGTGA CATGCCTGCT CCCTCTTTTG 1140
CCTTCTGCCA TGAGTAAAAG CTCTGAGGCC TCATCAGAGG CTGAGCAGAT ACTAGTGCCA 1200
CGCTTTGTAT AGCCAAACAA ACCTCGTTTC TTTATAAATT ACCCAGTCTC GGGTATTCTT 1260
TTGTGGCAAT GCAAAATGGA CTAACACACT GGCCATTAAG TGTCAGACTG AGAATTAAGA 1320
GCCTCTGACT GAGAAGATAG AAGTGAGAAC TCTGAGATAA 1360
|
