| Tag | Content |
|---|
EnhancerAtlas ID | HS131-00011 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr1:1079440-1080890 |
Target genes | | Number: 21 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:1080703-1080721 | GGAAGGAAGGCAAGGAGG | + | 6.93 | | Nr2f6(var.2) | MA0728.1 | chr1:1080757-1080772 | TGACCTCATGACCCC | - | 6.63 | | ZEB1 | MA0103.3 | chr1:1080366-1080377 | CGCACCTGCGC | + | 6.32 | | ZNF263 | MA0528.1 | chr1:1080701-1080722 | GGGGAAGGAAGGCAAGGAGGG | + | 6.1 | | ZNF263 | MA0528.1 | chr1:1080311-1080332 | CTCCCCTCCCTTCCCACCCCC | - | 6.23 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_10678 | chr1:1078154-1080826 | CD19_Primary | | SE_24482 | chr1:1077845-1081465 | Colon_Crypt_2 | | SE_24970 | chr1:1077814-1082618 | Colon_Crypt_3 | | SE_27531 | chr1:1078709-1080956 | Esophagus | | SE_28002 | chr1:1078456-1081135 | Fetal_Intestine | | SE_29232 | chr1:1078835-1080697 | Fetal_Intestine_Large | | SE_34473 | chr1:1079431-1080895 | HCT-116 | | SE_41856 | chr1:1079979-1080636 | LNCaP | | SE_52392 | chr1:1077928-1081420 | Small_Intestine | | SE_56870 | chr1:1078454-1081111 | VACO_400 | | SE_57937 | chr1:1079709-1080662 | VACO_9m |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1079486 | 1080150 | | chr1 | 1080566 | 1080748 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001142 | chr1 | 1077792 | 1081590 |
|
Enhancer Sequence | CCTTGTCTCC GCCCCTTCTC CCATCACACG CAGCCCCTTG AGAACAGCCA GCACCTGCCT 60
CCCAGGTCCG GGCAAGCAGC CTCCCCTCTC GACGGCCCCG GGCAGCCCCA TCACCCTCGG 120
CGGCTGCCCA GGCCCAGGCC TGTTTCCGGC CCTCCTCTGA GCACCTGGAG AGGAGGAAGT 180
GCGTCTTCTC TCCGGTGCCT CTGAGAGACA AGCCTACTCC CCCCGGGCTG GGTGGCCCAG 240
GGCACAGTTA GACCCGGGAG TGGAAAAGGC GGTGGCGGTT TTCTTGCTGT TGTCCCGGCA 300
GCGTCTTTGG TGACACTTTC CCGCCTTTGG AGACCAATTA CCCGGCAGAG GCCCAGTGGC 360
CTCATTAACT CTGCTGCGGC GTCGAGAAAG GGGGAAGGAG CCAGCCCACG GGCAGGGCAG 420
GGCGGCTGCA GACTCTCCCG CAGCTCAGGG GCCTGGAGAA ACCTGGCCAC ACCTGGCCCA 480
GCTGGGTCAG GCCTCTGCCA ACAGGAGCCC AGGGCCCCAG CGCTCCCCTC CCTGCCAGGG 540
AAACAGCCCA TAACGACAGC CTTTCCTGGA GCCTGGGTTG CATCAGCCGA GCCGCCAGCC 600
ACAGGGCCCC AGCAACGGCA CCTGGGCCCG GGGCCTGGCC TGCCGGGGAC ACTCGGCTGT 660
GCGCACCTCG AGGGGCTCTA CAGCCTGTGG GGCCGCGCCT GCCTCTCGGG GCTTCCGGGC 720
GATTCCTCCT TCTCCTCCGT GGTGTGTGCT GTGCAGACGG GGACCGGGCC AGGCCAGACG 780
CCGGATCCAG AGCAGCTTCC CAGACAGGCC ACCCACCCCT CCGAGGCCTC CCTCAGTCCC 840
CTGGCGGGAG TCCCCGGCCT TCCGGGCCTC TCTCCCCTCC CTTCCCACCC CCAGGAGGGG 900
AGAGGACTGA GGCCTGGGGT CACTGCCGCA CCTGCGCTCT GAGACCTGCA CTCGCCCAGG 960
CCGGAGTCCC CACGAGGCAG GAACCCTGGC ATGCGGCCGG CAGTGCCCAC AGCACCCAGT 1020
CAGCCGGGAG GGGTCTCACC CCACAGCCCC CCGCTCCTCC CCTCCACACC CAACCACAGT 1080
CCCTCCTGGC TGACACCGTG GCCCCTCCTG GCCTGTGCTC CCCGGGAACC TCAGTCAGTG 1140
TCACTTGAAC TCCAGCACCG GACCTGGCCC CGTCCATCCA GCCTCTGCCC CGAGAGCCCC 1200
GCCCGTATCT CCAGAGGACA CGCCCTGCCA GGGGACAGGC GGGAGCAGCT GAGGGCCGCC 1260
CGGGGAAGGA AGGCAAGGAG GGCATGTAAT CGCCTGACCA CATGGCCGAC CCCCTTGTGA 1320
CCTCATGACC CCCACCACCT TCATGGCCGA CCCCACCTGA CCTCATGGCC GACCTGACCT 1380
GACCGCACGG CTGACCCAAC CCCATCTCAT GACTGACCCC ACCTGACTTT ATGGCTCACC 1440
CCAGTGACCC 1450
|
