| Tag | Content |
|---|
EnhancerAtlas ID | HS176-32207 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr5:96228820-96229650 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr5:96229209-96229220 | CATGAGTCACC | - | 6.62 | | JUND | MA0491.1 | chr5:96229209-96229220 | CATGAGTCACC | - | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_11033 | chr5:96227461-96234009 | CD20 | | SE_18922 | chr5:96227172-96233747 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_63150 | chr5:96205179-96233880 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH05I096895 | chr5 | 96229141 | 96229290 | | GH05I096893 | chr5 | 96229408 | 96229925 |
|
Enhancer Sequence | TGCAAAATAA CTTATCTAAG GGCCATCTAT CAACACTGTA TTACATACAA ATGTGGAATT 60
GTAAAACTAG GTCTATAGAT ATTGGAGACT ATTCCCTCTA TTTCATTTCT GAAAACTCTC 120
AGTAATGCAG TAAATTATTA AAGTCACCAA AATTGTCTTT CACCAAGTGG GCAAATATCA 180
TTCTGTTGTA GAATCTGGTA AAATCTCTTA TTTAAAACAT TTTAACTTTA TCCTTTATCG 240
TCACCACAAT AATGAGCTGT TGTTCTTTAA AGCAGTGAAC TAAATACTCT GTTACACAGA 300
GAGCCATGCT CAACACTGTG CTTCGAGAAC ACATGGGCTG CTTCCTTTGG TTCAAAATCT 360
CCCCACTGGC GCATTTTAGG TGTTTTGATC ATGAGTCACC AGGAGCTCTA AAGCACTTAA 420
CTGAGTCTGG GGATTTCTAA TCTTTCTGCC AGTTGTTTGT AGGGAAGTGC TCTGTGAGCT 480
CTACCTCTGA GGCTCCATGC TCCCTCTGGC CCTCCCTTTA ATAGCTTCTC TTCCACGGAG 540
ATGCAGTCAA GTGCTGAAGC AGCAAACAGC ACTGGAATTT TTGCCCCCAC TTTTTTGTCT 600
TCCCATTGAT TACCATGTTA ACATGTCACT CTGTGCATAA CCCTGGCAAA GATTTCCTCA 660
TGCCAACTGT CTTAGCTTGG CATACAAGGT TCCCATGACC CAGCTCCTTT TTACCTCTCC 720
ATCCTCATCT CTTGCCTACA CCTAAGCTTT AGCCATCCAA GATTACCTGC CATTTTCTGA 780
ACATGCCAGG TTGTATCACT CTGCCTTTGC TCCTACTACC TGATATTCAG 830
|
