| Tag | Content |
|---|
EnhancerAtlas ID | HS147-05180 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:246776210-246777120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:246776965-246776986 | CCTCTCTACCTCTCCTCCTCT | - | 6.05 | | ZNF263 | MA0528.1 | chr1:246776962-246776983 | CCTCCTCTCTACCTCTCCTCC | - | 6.26 | | ZNF263 | MA0528.1 | chr1:246776980-246777001 | TCCTCTCTCCCTCTCTCCCTC | - | 6.41 | | ZNF263 | MA0528.1 | chr1:246776984-246777005 | CTCTCCCTCTCTCCCTCTTCC | - | 6.76 | | ZNF263 | MA0528.1 | chr1:246776946-246776967 | TTCTCTCTCTCTCTCTCCTCC | - | 7.1 | | ZNF263 | MA0528.1 | chr1:246776949-246776970 | TCTCTCTCTCTCTCCTCCTCT | - | 7.26 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_18768 | chr1:246775841-246777251 | CD4p_CD25-_Il17-_PMAstim_Th |
|
| | 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 |
| GH01I246612 | chr1 | 246775842 | 246777251 |
|
Enhancer Sequence | AACTCAGTGT TAGGGACATA CAAAGCTTAA CTAATTGAAA TTTGCTGAGT TTTAAAACAT 60
AGTTCTCGAG CATTTATTAT TTACTATATG CCAGCCACTG TGGTACATGC TTTATGTGGA 120
TTATCTCATT TACTCCTTGT CACAATCTTA TCAAGCATAA TACAATTAGC TCCAATTTAT 180
AGATGTGGGA TCTGAAGCAC AGAGAGATTA AGTAACGTGC CCGATGTCAT TGCTGAAAAG 240
TGTATCACTG AGATAAAGTA CATCCCAGGA CTTCATCCCA GGTAGTCTGA CTTCAGACTT 300
TGTGTCTAAT GGTTAAGCTA TACTATCTCA CTTTTGCTGA ACTTTAAAAG TGTGCTTAAA 360
GCAATACATG ACTTTCCACA ATTTGCCGCA GAACAATTAT TGCACATTCC TTTCCTCAGG 420
GTGTGTTGGT GGCTATGATT CCTGCCTGCC AGCCTCAGCA AGACAAAACA CAATCAGAGA 480
AAAGGTGGAT GGTTCACTCT TAAGGGAAGT AGTGGATTTG GGTTTGTTTC AGTAATCGTC 540
TCTGAATAAT GGCATAACCT TCTCTCAGAT TTTTAATTTG ATCTAGTTTC ATTGCAGTGA 600
AAGGAAGCTT TAACACTTGG ATCAAAGAAA GTATTTGTAT AAAAGCAGCG AATGTAGTTT 660
TGAATGATAG GGTACTTGTA CTCTGAATAG TAGTATACAA TATTTGAACT GTATGAGGCC 720
TTTTTTTATT CTTTCTTTCT CTCTCTCTCT CTCCTCCTCT CTACCTCTCC TCCTCTCTCC 780
CTCTCTCCCT CTTCCCGTCT CCCTCTTCTG AGTCTAGCTT TGTCTTCCAG GCTGGAGTGC 840
AGTAGCCTGA TCTCGGCTCC CTGCAACCTC CACCTCCCAG GTTCGAGTGA TTCTCCTGCC 900
TCAGCCTCCC 910
|
