| Tag | Content |
|---|
EnhancerAtlas ID | HS105-58894 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr3:187703880-187705010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr3:187704432-187704443 | GGATGACTCAG | + | 6.32 | | JUNB | MA0490.1 | chr3:187704432-187704443 | GGATGACTCAG | + | 6.14 | | Nfe2l2 | MA0150.2 | chr3:187704430-187704445 | AAGGATGACTCAGCT | + | 6.06 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_25506 | chr3:187703341-187706506 | DND41 | | SE_31029 | chr3:187703153-187706454 | Fetal_Thymus | | SE_39559 | chr3:187703777-187704879 | Jurkat | | SE_58285 | chr3:187606861-187725246 | Ly1 | | SE_59604 | chr3:187596115-187720147 | Ly4 | | SE_60392 | chr3:187615879-187719658 | DHL6 | | SE_62680 | chr3:187634828-187719022 | Tonsil |
|
| | 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 |
| GH03I187985 | chr3 | 187703561 | 187706231 |
|
Enhancer Sequence | TCCTGGGTTA TTTATCTCCA TATCCCCCAA GAGGGCTCTG CCTGTAGGTA GTACTCAAAT 60
AATATTGAGT GAATAAATCT AAGGATCAAA GGTTTCCATC ATGAGATGCT GAGCTCCTTG 120
ACAGCAGGAA CCCTCTATTA ACCCCTCTGG CACAGTGTGT TGCACATAGT AGGTACTAAA 180
CTGTGAGTTG AATCAAATGC CATCCTTTCC CAGAGATGAT GTAAAGAGGC AAAGTAATAT 240
ATTGGAAATA GTGTAAACTT TGAAATCCTT CAGGTCTGTG TGGCCTTGGG AAAATGACTG 300
AACCTCACTG AGCCTCATGT TCCCCATCTG AGGATAACAC CACTGCCTAA GACAATTGTG 360
ACAAGACATA AATGTTGATG AGTCTGGCAT TGGCGTGGCA CACAGGAGGT ACCCAGGCTA 420
CATCAGCTCC TTTTCTCTCT TCTTTCCTGA AGTCACAGAG ATTGTCCAGC AGATGGGAAT 480
GTCCATGCCC AGTGGCTCAT GCTCAAACCC TTTCACCCTG ACACAGTGCG GGGAGACAGG 540
AATAGGCTCG AAGGATGACT CAGCTCCAGT GACTAAAGCA AGGAGGTGGT GGTGGTAGGA 600
ACGGGGTAGG GGCTAAAAAG GAAGTGAGTT AACACTATAT CTGATGAAGG ATGACTCCAA 660
AATAAAAAGG GGTTGGCCCT AGCTGGTTCC TGGCTCTGAA ACGGTGCAAG TGAACAGGGG 720
CCTGAGTGCT TCTCCATGAC TCCCTCCACC TCATCTCGTG GGGAACTCCC TGCCTACCCA 780
GGGATGTCTT CCAGAACAAA TGCTGAGCAT TCTCTCTCCT CTGGAGGCTT TCAGACCAGG 840
CACTAGAGCA CACTTGAATG CCACTTTTGA TGGAGTGTTT TTTTAAGAAG TATCCCGTAT 900
GACTGAGATC AGCGTGCATG GATTCTAATC CTGACAGCCA CCTGGGCCTC TCTCCTCGAC 960
TCCAGACAAT CTTTTCCACC CACACCACCA CTTTGAAATC CCCAAATATT GCACATGCAG 1020
CAAGGTTAGA CCAGTCTTCC TGCCTGCAGG GTCACCCCAG TCCATTTTCT AGACTGTGCA 1080
CAGAATGATA TGTTCAAAAC TAATTTATAA TTCTGCTATC CCTCTGCTTA 1130
|
