| Tag | Content |
|---|
EnhancerAtlas ID | HS073-07198 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr19:6641210-6642550 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr19:6642070-6642091 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | Nr2f6(var.2) | MA0728.1 | chr19:6642294-6642309 | TGAACTCTTGATCTT | - | 6.07 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_18687 | chr19:6641109-6642700 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19251 | chr19:6641137-6642851 | CD4p_CD25-_Il17p_PMAstim_Th17 |
|
| | 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 |
| GH19I006641 | chr19 | 6641339 | 6642579 |
|
Enhancer Sequence | CCTGTATTCC CAGCAACTTG GGAGGCTGAG GCAGGAGGAT CATTTGAGCC CAAGAGTTTG 60
AGGCTGCAGT GAGCTATGAT CGCACCACTG CACTCCAGCC TGGCTGACAG CTGGTCTCTT 120
AACAAAAACA ACAACACAAG TCTATTATCT TAAAGTTCTG GAGCCCAGAC TCCAAAATCA 180
GTTTCACCAG GCTTCTCCCT GTGATTTTTC AATCCAGGGT TAAATGCACT CCAGGCTGCT 240
GGAGTGCAGT CATATGATCG TAGCTCACTG CAGCCTTGAA CCCCTGGGCT CAAGCAATCC 300
TTCTGCCTCA GACTCTCAAA GTGCTGGGAT TACAGGCATG AGCCACCACG CCCTGCCCTC 360
CCTGTGTCTT TATAAGATGG TCCCTTTTTC TGTATCCCTG TCCTAATCTC CTTTTCTTAT 420
ACAGACCCTA ATCTTATTGA ATTGGAGCTC ATCTTAAGGG CCTCATTTTA AGTTAATTAC 480
CTTTTCGAAG ATTCAATCTT CAAATACAGT CAAATTCTGA GGTGGTGGGG GCGAGGACTT 540
CAGTGTGTAA ATTTCGGGGG AACATAGTGA GGCCCGTACC ATGGAGGAAA GTTCCTACAC 600
CCTGCTTTTT AGGTAGAGAT CTAGAAACAT GGAAAGTTCC CCAGAGGAGT TTTAGAGGAA 660
CCTAAAGATA GAGAAGGCTT GGACTCTGCT CACCACAACA GAGACCAGAG AAGCGGCAGG 720
TCTCCAAAAA AGGAAGTGAC TTAATAGTGG CTTTGGGCAT CTGAAGCCAC AGAAAGCCTC 780
AAAAAGTTTC CTGTGCCTCA ACTCAGCTGA AAATCGGCCT CACGAGCAAG GTATAGGAGT 840
AGTAGAGAAA GTGCTGCCTT TCTTTCTTTC TTTTTTTTTT TTGAGACAGA GTCCCACTCT 900
GTCACCCAGG CTGGAGTGCA GTGGTGCGAT CTCTGCTCAC TGCAAGCTCC GCCTCTTGGG 960
TTCAAGCGAT TCTCCTGCCT CAGCCTCCCC AGTAGCTGGG ACTACAGGTG TGCACAACCA 1020
CGCCCAGCTA ATTTTTGTAT TTTTAGTAGA GGCGGGGGTT TCACCGTGTT AGCCAGGATG 1080
GTCTTGAACT CTTGATCTTG TGATCCACCC ACCTCGGCCT CTCAAAGTGA TGGGATTACA 1140
GGCGTGAGCC ACCACGCTCA GCCAAGGCGC TGCCTTTCTA AGGAACAAGG ACAAGAAAGA 1200
AGGTCTCATA GGCCAGGAGC AGACGGATGG TGGGGACCTT ATGGACATGC ATTTTGAGAA 1260
TTAGTCTTTT CTTCACCCTT AATGCCTCCG CAATTCCAAA GCTCCCTGGA ACTTTGACAG 1320
TCTTGGGAAA GCAGGATGTA 1340
|
