| Tag | Content |
|---|
EnhancerAtlas ID | HS187-21136 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:36659380-36660600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr6:36660187-36660201 | AGAAAGGGGAAGTG | + | 6.22 | | SPIB | MA0081.2 | chr6:36660189-36660201 | AAAGGGGAAGTG | + | 6.07 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09785 | chr6:36658984-36661639 | CD14 | | SE_10510 | chr6:36658788-36661575 | CD19_Primary | | SE_11108 | chr6:36656796-36663991 | CD20 | | SE_27338 | chr6:36659435-36660995 | Esophagus | | SE_29503 | chr6:36659013-36660538 | Fetal_Intestine_Large | | SE_59249 | chr6:36634013-36660855 | Ly3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 36659494 | 36660539 | | chr6 | 36660058 | 36660307 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I036691 | chr6 | 36659160 | 36660977 |
|
Enhancer Sequence | GCCAACCAAC CCCATAATCC TTATCATTAC TATTGCCCTG TATCTTTCAA GTATTAGACT 60
TACAGTGTAA GTCAGTGTTG CCCCTGAAAT TTTACCTGTG CCTCATCCCA ATCCACTACA 120
CACATTGTGG ACACTGTGAT GCTGTAGTCT GCCAAGAGTT ATCACCACCT TACTCACTAC 180
CAGCATTTGG GTCCGCGTTG TCACTTCACT GGTGAGGGAT CTGTTTTCAG AAGCCCATCC 240
TGCTTCTGCC ATTTCTGGTA ACTGTCTTAG TCACCCCCAA CCCCCACTCC CCAAACAACT 300
TGAGACAAGG ACTTGTGTGC AGGTGGAATG CCTGGGAGGT AGTCCCTGGA GGCACAGCAG 360
GAAAGTAGAG AATGTGAGAA AGAAAAGGAG AAGGCCAATA AAGGTGTCAG TGAACAAGTT 420
CCACTGTGTG CAACTGGGGC TTAAACCTGC TAGGGAGCCT CAAGGAAACC GTGTGGAACA 480
CACCCTACAA TTTTCTCTCT GGAGTACTCA CCTGGCTATC TAGGCTACTT ATCTAAGGAC 540
ACTGTCCATC ACTGATAGGG CTGCCTCTAG GGCCTAGTCC AGATTGCTCC TCATGGGGTG 600
GAAGAAATTC CTGTAATGGT GAAGAAAACC AGAGGGATGA AGACATTTGA GGTGGGAAAT 660
CATTAGCCTG CCAGGAACTA TCTACCAAAG GTTTAGGTGA ACACAGATAT GGGCCAGATA 720
GTGCCTGAGC TCACGCCCCT AGGAAGTGGT GAGGGGCCAG GATGTCCACG CTGATGACTC 780
CAGATCACAC TGCCTGCTCA ATACACCAGA AAGGGGAAGT GCCTCACCCA GGGCCACTGC 840
TGCCGTGACA ATTCTAAGAG GAGGCTTGCA GGGACCCACC TCTTTCTGTG CACCTCCTCA 900
GTCTTTGATG TAACTTAGGT TTTCTCAATC TTATGTAAAA TGCTACCCAA ATGCAGCTTT 960
GAAGCAAGCT CCCTGACCCT GGTTTTCTGT GGGATTGCCC ACCTGCCTAA GCTCCTTGAG 1020
CTATTTTGGA GTCAGTAGCT GGAGGCAGGG AGGCTCAGGT CCTAGCTTGC ACATCAGCTC 1080
ACACTGCAGG GCCCTAGAAT GGAGAGTTTG TTGCTTCAGG ATTTAACAAG CTGTGAAGAG 1140
CTTTCAAGCA TCTGTAAGGA ATTAAAAATT AGTGAGTGTG AAAACTTTCC TAATTGTAAA 1200
ACAGTTTCAC TGCCCTTGAT 1220
|
