| Tag | Content |
|---|
EnhancerAtlas ID | HS182-20530 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr8:11275270-11276280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr8:11275577-11275592 | GGGGCTTTGTGACCT | - | 6.02 | | RARA(var.2) | MA0730.1 | chr8:11275493-11275510 | AGGTCGACCAGAGGTCA | + | 6.65 | | STAT1 | MA0137.3 | chr8:11275322-11275333 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr8:11275322-11275333 | TTTCTGGGAAA | + | 6.32 | | Stat4 | MA0518.1 | chr8:11275322-11275336 | TTTCTGGGAAAGGG | + | 6.56 | | ZNF263 | MA0528.1 | chr8:11276048-11276069 | CCTTTATCTCCTGCCTCCTCC | - | 6.55 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_58515 | chr8:11271776-11367112 | Ly1 | | SE_60559 | chr8:11246636-11318640 | DHL6 | | SE_65314 | chr8:11275329-11276524 | Pancreatic_islets |
|
| | 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 |
| GH08I011416 | chr8 | 11274097 | 11276396 |
|
Enhancer Sequence | TTCTAGTTAT TTCTTGATCA TATGCTAAAC AAGGGATAGA TTATTCATGG ATTTTCTGGG 60
AAAGGGGTGG GGAAATCCTG GAATGGAACA GAGGGTTCCT GCCCTTTTTA GACCATGTAG 120
GGTAACTTCT GGCCTTTGCC TGTGGCATTT GTAAACTGTC ACGGGGCTGG TAGGCGTGTC 180
TTTTAGCAGC TAATGCATTA TAATTAGCAA ATAATAAGCA GTGAGGTCGA CCAGAGGTCA 240
CTTTCATTGC CTTCTTGGTT TTGGTGGGTC TTGGCTGGCT TCTTCACCAC ATCCTGTTTT 300
ATCTACGGGG GCTTTGTGAC CTGTGTCTTG TGCCGACCTC CGATCTCATC CTGTGGCTAA 360
GAATGCCTAA CTTCCTGGGG ATGCAGCCCA GCAGGTCTCA GCCTCATTTC CCCCAGCCTG 420
TTTGAGCCGC AGTCGCCCTG GTTCCAATGT CCCTGACAGT AACGGGCACC CCTTTAGCTG 480
CACCCTGCCT TCTTGCCTCA AGGAGGAAGT GCCTGGTCCT GTTCTCTGAG CCGGGTCTCC 540
ACTCGCACTC TGCCGGGGGT TCTCTCCCCT CCTCCAGAGC TGCAAGTGCT GTGGCTGCCC 600
TCTTTCCTGT GCACATCGTC TCTCTTTCAG CAGGCACTGA CCTATCTCAC ATGACAACAC 660
CTTCATTATA TTATACGACG TTATGAGAAA ACCACAAGCC ACTTTCTGGA CCTTATCTAT 720
GTCCTTGTCC AGCTCCTTGT CTCTGCTCCC TTTATGGCAC ATGGATGCAG CAAGGTGGCC 780
TTTATCTCCT GCCTCCTCCT CAACCCTGGC CTTACCACTG AGCTGAGATG GCCATCTCCC 840
CCATCACTGC CATCACGGTG GAGGAGGGGC TCCCTCTTGC TGAAGCCAGC ATCCACCTCT 900
CTGTCCTCTT CTTCCTTGAT GTCTTAGCAG CGCTGGTGTA GACGACTCTC TCCTTCAAAC 960
AGTTTCTTCC TGAAGGCTGC CGGATGCCCT GTCCAGCTGC TTTTCCTTCT 1010
|
