| Tag | Content |
|---|
EnhancerAtlas ID | HS156-02018 |
Organism | Homo sapiens |
Tissue/cell | P493-6 |
Coordinate | chr11:47397280-47399850 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:47398186-47398204 | TCCTCCTTCTTTCCTCCC | - | 6.07 | | NR2C2 | MA0504.1 | chr11:47397479-47397494 | GGGGGTGAGAGGTCA | + | 6.94 | | ZNF263 | MA0528.1 | chr11:47399507-47399528 | GTCCCCCCATCTCCCTCCTCT | - | 6.09 | | ZNF263 | MA0528.1 | chr11:47398189-47398210 | TCCTTCTTTCCTCCCACCTTC | - | 6.32 | | ZNF263 | MA0528.1 | chr11:47398196-47398217 | TTCCTCCCACCTTCCTCCCTC | - | 6.34 | | ZNF263 | MA0528.1 | chr11:47398119-47398140 | GTCTCCTTTGCTTCCTCCTCC | - | 6.38 | | ZNF263 | MA0528.1 | chr11:47398193-47398214 | TCTTTCCTCCCACCTTCCTCC | - | 6.48 | | ZNF263 | MA0528.1 | chr11:47398162-47398183 | TCCTTTTCTTCCCCCTCTTCC | - | 6.61 | | ZNF263 | MA0528.1 | chr11:47398122-47398143 | TCCTTTGCTTCCTCCTCCCCC | - | 6.76 | | ZNF263 | MA0528.1 | chr11:47398171-47398192 | TCCCCCTCTTCCCTGTCCTCC | - | 6.97 | | ZNF263 | MA0528.1 | chr11:47398200-47398221 | TCCCACCTTCCTCCCTCCTCC | - | 7.05 | | ZNF263 | MA0528.1 | chr11:47398215-47398236 | TCCTCCCTGTCCTCCTCCCCC | - | 7.4 | | ZNF263 | MA0528.1 | chr11:47398128-47398149 | GCTTCCTCCTCCCCCTCCTCA | - | 7.59 | | ZNF263 | MA0528.1 | chr11:47398131-47398152 | TCCTCCTCCCCCTCCTCACTC | - | 7.68 | | ZNF263 | MA0528.1 | chr11:47398174-47398195 | CCCTCTTCCCTGTCCTCCTTC | - | 7.87 | | ZNF263 | MA0528.1 | chr11:47398209-47398230 | CCTCCCTCCTCCCTGTCCTCC | - | 7 | | ZNF263 | MA0528.1 | chr11:47398074-47398095 | TCCTCCCTATCCTCCTCCTTC | - | 8.29 | | ZNF263 | MA0528.1 | chr11:47398212-47398233 | CCCTCCTCCCTGTCCTCCTCC | - | 9.14 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_09161 | chr11:47394847-47401444 | CD14 | | SE_11270 | chr11:47394895-47403073 | CD20 | | SE_13558 | chr11:47395058-47401199 | CD34_Primary_RO01536 | | SE_42327 | chr11:47397093-47400940 | Lung | | SE_53339 | chr11:47395223-47401122 | Spleen | | SE_59674 | chr11:47395040-47431135 | Ly4 | | SE_61805 | chr11:47397401-47437798 | Toledo | | SE_62612 | chr11:47395047-47423503 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 47397800 | 47397933 | | chr11 | 47398240 | 47398586 | | chr11 | 47398625 | 47399055 |
|
Enhancer Sequence | CTGCTGAGAG AGGAGGTGTC AGGGCCTGCA CCATGGTGGG AGACCCCAGC CAGGCCTGCA 60
GCACCCCCGC ACGCTGGGTC CCCATCACCT TCCCTGGCTC AGTGGCTGCG TTGGACCTAC 120
AGCCCTCCCT CTGCCTGGAA CTGGGACAGA GAGTGGGGCA GGGGACCCAG AAGGCCTGAA 180
AAGGGGTGAC AGGGACCTTG GGGGTGAGAG GTCAGAAGAG GACCAGGGTC CCCCTCTGCT 240
GGGCTACTCC CCATAGCCAC CTCACGCTCA CACTCACACT CACGCCTGTG TGCCCCCATC 300
CTCATCCCAC ACACCTCTCC TGGTCACACT GATGCACATG TCCACACGAT CCCTGTGTCA 360
CCCTCACACT CATAATCCCA CACGAGGACT CACTCTCACA GCCCCTACCC ACCCCCATGC 420
AGGCGCCTGC ACACTATCCC TCACACACAC ATCTTCATAC CCACTCAGAG GTCACCCACC 480
TCACAGAGAC ATTGTACACT CAGCTCATGC ACACACGCAG AGTCTCCTTG ATTGACACTC 540
ACATGACACC ACGTTCCAGC CATCAACACA CACACTCACA CCCCCAGAGC CACTCACATT 600
CCACCTGCAC ACTCAACCGC ACAGCACACA CTTGCCTGCC CAGCCCCACT CTCACAGCCT 660
ATGCCTCTCA CACAGCCTGG GCAAGAGTGG CACCACAATG ACCCTCCACA CTGACGGTTG 720
GTGCAGGGGT CACCCAGGCA GACTTAGGGG CCGAGCGCAT GGAGGGCCTT GATCCCCTCA 780
CTCTCCCTCC TGAGTCCTCC CTATCCTCCT CCTTCCCTCC TCACTGCATC CCCCTCCCCG 840
TCTCCTTTGC TTCCTCCTCC CCCTCCTCAC TCCCCTCTGT CCTCCTTTTC TTCCCCCTCT 900
TCCCTGTCCT CCTTCTTTCC TCCCACCTTC CTCCCTCCTC CCTGTCCTCC TCCCCCTACT 960
GGCACAGACA CAGGGCCGTG CACACCCAGG AGCCTTCCCA ACAGTCATCA GGCCTCCCCG 1020
CCCCCGCAGC GTGTGGCCCA GGATTGCATA ACAGTCACTG TGGCCCTTAG GGCTGGGCTT 1080
GGGGGACCGG GGCTGCCTTG GGAGCCCACC CTACCAGGAG ACACTCAGAG TGACCCTGGA 1140
GCTTGCAGAG AGGGCTGGGG GTGCCTAGGG ATGGCCCAAG GAGCTCTGCC ACCCATCTAG 1200
CTCCACCTGG AGTTCAGAAT TGAGAGGTCA GGGATCAGAG ACAGTGGGCC TGTGGCTTTC 1260
TTGAGGCAGA ATTGGCTCTT TCTGAGACAA CCTCCGTCAC CCTCTGCCTG GGCCGCCCAC 1320
TTCGTGTTCC CAGGTGGGAA GGGGTGTCGG TGTGGATGCC ACAGCAGGCT GGCTGGTCCT 1380
GCCTGGTCCT GCCTGTGGCT GGCCAAGTGA GGAGGCCAGG AGCCCAGCAC TGAGCCTGCC 1440
CCTCTGGGTT TCCAGGTAGT ACAGCCTCGC TGCAGGATGT CAGCCCGGCT CTGGTCGGGT 1500
TGGTGTGATG TCAGGCCTGG GGTGCCTCCC AGCCTCCTGG GGTGGCTCTG AGCCAGGGCA 1560
TAGTGGGGGA AGGGAGCTGC CTCTAGACCA GGAAAGTGGA TTCAGGTGGG CAGCCTGCCA 1620
AGCCCTTCCC GGCTCCCCTC AAGCCTCCTC ACTCCTGAGA GGTCATGGGG TGGGAAAAGG 1680
GAGAAGGGTC CTTTCCGAGG GACCCTGGTC TGACACCTGC CTAAGGCTGC AACTGTCACT 1740
GAGAGTGAGG AGCAGTGGCG ATCTGCCCTT CTCTTCTCGG GGTCCCCTGG GGCTCCCACT 1800
TCTTCACCCC CAAGACCCAG TCCCTGTCCT TGTCCCAGCC TCAGCCCCCA TTCTCACTTA 1860
TCACATGCTC ACCCCAGGTC CCACCCAGCC CCAATCTCAG TCCTGGCCTT GTCCCAGCCC 1920
TGTCCCCTGC CGCGCCTCTC CCTGAACTCC AGCCCTGGGG CCAGCCCTAA CTGCACTGTC 1980
TCAGCTCCAC TCCTGGCTCC TTTCCAGCAC CAGTCCCTGT CTCCTGTGGG TACCCCTGTG 2040
GGCCCATGGC CCTGACCCTT TGGTCAACAA TCATGTCCTC TGTGCCAGGC CCCAGACTGG 2100
GCGTTGGGGA CCCAGAGTTC CATCAGCTTT GGTTTCCAGG AGCCCCAAGG CCATGGGCCA 2160
AGACTTCTGC CCATTGCCTC CTGCCTTCAA CCCCTTCCCA TCCAGGGGAC CGGCCTCCCC 2220
CAAGCCAGTC CCCCCATCTC CCTCCTCTAC CTCTCTACCA CCGCCTTCAC CATCCTCAGC 2280
CCAGCACCCT CCCCAGGAGC CCCGGCCTCC GCCTGCCACC CGAGCCCTGT CTATAAATAA 2340
CTGTTCAGGC CCCACCGATC ACAGCCCCAC CGTGGGCCTG GCCTCAGCCC GCCAGGGCAT 2400
GCTCCGAGGA AGCCAATGGC CCCCTCGCTG GGTCTCAGGC CAGGAGTTCC AGGGAGGAAA 2460
CCCTGACTTC CCACTGATAG CAAGCCAGGA GGGCAGTGGG TGGGCTGGCG GGTTCGTGGG 2520
CAGGCAGGCA GGCGTCCGAG GGCCACGGGT TGGGCTGGTG GAGGAGTCCC 2570
|
