| Tag | Content |
|---|
EnhancerAtlas ID | HS073-14276 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr9:33128660-33131640 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr9:33129997-33130011 | TAAAAGAGGAAGTA | + | 7.06 | | SPIC | MA0687.1 | chr9:33129997-33130011 | TAAAAGAGGAAGTA | + | 7.73 | | SREBF2 | MA0596.1 | chr9:33128973-33128983 | ATCACCCCAT | - | 6.02 | | ZNF263 | MA0528.1 | chr9:33129892-33129913 | GGAGGAGGAAGTGGCTGGAGG | + | 6.59 |
|
| | Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
| SE_00330 | chr9:33131315-33133010 | Adipose_Nuclei | | SE_09459 | chr9:33129171-33132533 | CD14 | | SE_10229 | chr9:33127769-33131935 | CD19_Primary | | SE_10912 | chr9:33119344-33169982 | CD20 | | SE_12090 | chr9:33130620-33131585 | CD3 | | SE_18665 | chr9:33129793-33132844 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19329 | chr9:33130392-33131632 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20045 | chr9:33128349-33132443 | CD56 | | SE_22416 | chr9:33128783-33132526 | CD8_primiary | | SE_26031 | chr9:33129309-33132935 | Duodenum_Smooth_Muscle | | SE_26859 | chr9:33129122-33131571 | Esophagus | | SE_27770 | chr9:33128137-33132419 | Fetal_Intestine | | SE_28724 | chr9:33128066-33132484 | Fetal_Intestine_Large | | SE_31534 | chr9:33128891-33131746 | Gastric | | SE_32659 | chr9:33129028-33131615 | GM12878 | | SE_35029 | chr9:33129460-33130398 | HeLa | | SE_35029 | chr9:33130436-33131878 | HeLa | | SE_40894 | chr9:33128725-33131858 | Left_Ventricle | | SE_41831 | chr9:33129685-33130482 | LNCaP | | SE_41831 | chr9:33130578-33131658 | LNCaP | | SE_42236 | chr9:33128546-33131800 | Lung | | SE_44340 | chr9:33130634-33131475 | NHDF-Ad | | SE_45731 | chr9:33130368-33132932 | Osteoblasts | | SE_47814 | chr9:33129311-33130060 | Pancreas | | SE_48738 | chr9:33128803-33130531 | Right_Atrium | | SE_48738 | chr9:33130653-33131691 | Right_Atrium | | SE_50176 | chr9:33128355-33131838 | Sigmoid_Colon | | SE_52621 | chr9:33128937-33131899 | Small_Intestine | | SE_53402 | chr9:33129123-33131619 | Spleen | | SE_58985 | chr9:33124740-33168862 | Ly3 | | SE_62118 | chr9:33106994-33169093 | Toledo | | SE_62346 | chr9:33106942-33169226 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 33129600 | 33131200 | | chr9 | 33129527 | 33131297 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I033127 | chr9 | 33127964 | 33132882 |
|
Enhancer Sequence | CTCCCAAGCT CCGTTCCCAC ACACATCAAT CTGTGCACTG ACAGCTGAGG TAGAAAATGG 60
AAGGCCGGGA TGGGGGGATG GTAGAGATGA TCAAGATAGA AACCAAACCA ATGAGGCCAT 120
AAGCCCAGGC AGCTGTCCTC ACTAATGGGA TAGACCCAGG AGTCTGCTTC TCCCCAGTTG 180
ATCTTGACCT TGTGTAGGAA CCAGCTGCTT GGACCAGTGA CAGAGACAAC TGCTGAGGTA 240
GGGTGACAGA TACTCTTGCT CACTGAGGGT ACAAAGGACT GTCTCCAAAT CCATCCTCAA 300
CCAGCCTGGA ACTATCACCC CATCATCCTA AAACAGTGCA CAGAAGAAAA GGAAACAGTA 360
GAAAACTTCA AAGCCAGACA GAGTCCTCAG GGCAGCCCTC CCTCCATTTC TCCACAGCCT 420
TTCAGGCAGG CTCCAGCTCT GCTTCCTGGC CATCGTGTGC TTACCTGTGG AGCCTTCCCT 480
CTGCAGGAAC AATCAGAAGA CCATTTGCCT TACTCTGGGG GATGGGGGGA GGTGGGAGGT 540
TCAAAATTCA AAGTGAGACC ATAAAGGTGC TGAGTCCAAA GGACCCTAAA GGAGTTTTGT 600
GACCATTAAC AATCACAAGG CTAAGGTATT AATAGGTTTT CTGCATTTTT CCTGATAAGG 660
GAGGTCACCC CAAGGACTGT CACAGGCAGC CTGTGCTCTG GTCAGCATTG AGCTGGAAGC 720
TTCGGGGAGA GGCCCAAGGG AGGGATCCTG CAAGTTCCCA AGGGTCAGGA CCTGGCCCCA 780
CTGGGAACGG AGGCTTCACT TCCAAGAGGC ACAGATTTAG GCAGAAGACC AGGAGTAGGG 840
AGTCCTGAGA CTAGGGATAA ACAAAGGGGC AGGAATCCTG GAGAGAAGCC CCGTGCTCCA 900
CTCACTGACT GCGTCTGTAC TGACTATGTA CCAGCTGTGT GGTCAGAGAG AAAGAAGGGA 960
GGCAGACATG AGGGACTCAG AGTCCGGGGG CTGGGGTGAG GCTGGAACTC AGATAATCAT 1020
CCCTTTCCAG AAAGTTCTGA GCAGCCTGGG AGCAGCAGGG AAGGAGAAGT CAGCTCTATT 1080
CCAGGGGCTC CACAGAACTA ATGAGGTTGG GGAGGGAAGC TTAAAAGATA GCCAGAGACA 1140
CACTAGGAAC ACAGGGGACA GCATAAGCAA AGGCACACAG AGGGGAGAAC AGAGGTGTCT 1200
GGGTGGAGAT GGGGAGTCCA GTGAAGTGGA GAGGAGGAGG AAGTGGCTGG AGGTAGGTCA 1260
GGGTCTCGGA TGCTAAGCTT GGGCCTTCCG ACCATTTAGA CCGTTGCCTG TAGGCAGTCG 1320
TGAAATGCTA ACAGGTTTAA AAGAGGAAGT AACATGGTCA GAACCAGAAA AATCCTGGGC 1380
AGCTGAGGGA GAGGAACAGA GGTGCCAGAA GATATGCAAT CGGAATTGGA GAGACCAGTT 1440
CTGTGTACTG GCTGTGGGGC AAAGGGCTGC CATGGTTGTG ACAAACCCAC CTGGCCAGCT 1500
GTGCCTGCAT TCCTTACTCA TTTTGTAATT TTTATGATGG GCAATCCCAC AAACATTCTG 1560
CATTCCTTAA TTTAGGGCTA GTGCTACCAG GTGGTGACCT GCCCTCCCTT CACCTTGAGT 1620
GAAGTCTCGT TTCCGGGTTT GAGTATTAGG AAATGCAGCA TGCATCCCTG TTTGCTATGA 1680
TGTCTTCTCC TTCTGTTGCT TCTTTTCTTG CTGCCGTTGA AGTTGGAATG CTATATCTTG 1740
AAATCCACGT CTCAGAGTAC AAGGAGTCAA ATAGTATTCT CCCATGCTGG TGAGCTAAGG 1800
TCAGGGGTGG GAGGAGAGAC CTTAAGGAAA AAGAGCAACT CTTGTTCTTC TATATCTCAA 1860
CCAGGAAAGC CTCTCCCGGC TCATTCCTTC AATATCCTTA TTTTAAGATA TAAGTTAGTA 1920
CAATAATTAC AGAGGCATAA GCCAAATGGG AGTGGTTAAC AGCTTACTAT AGACAGAGTA 1980
TGAGTCATAA CAACTTGTGA AAGTTCACTC CTGTGTGTAA AGCTTGATAC GTGGCCCTAT 2040
TTTGAAGAGG CTTATAGGCC CGGGATGGCC TCTGAGATTC TGCCACCTGG CTCACTCCAC 2100
TATCCATTAC CCTCTGACTC CAAGGAGTTC AAACCAATAG GAGGAAGGGT CCTGATGCGG 2160
GCCCTGAGTG GGGGTGCAGC AGGAGGCGGT GGGAGCCATG AAGAATTCAC CACCACAGAA 2220
GCAGGCAGAG GAAGCAGGCA GAGGAAACAG GCAGGATGAA TGGAGAGTGG AGAGGCAGGA 2280
GTGGACCCTC CTAGTAACGG CTGGTATTTA CTGAAGGTTT ACCATGAGAA GGATGCCTCA 2340
TAACCCTCCC CACCAAGGAG GAAACTGAGG CCTGCAGAGC TTAAGTAACC TGCCTGAGGT 2400
CACTGACTGT AAAGTGGCAG TGCCAGGACT GAACCCAGGC AGTCTGAGCA CACAGCACAC 2460
TCTCAGCCCT GGATACCAGA CTGTGAGCAA CACTGGGGGC ACCCTGGCCA TGAGGAGTGT 2520
CACTGATGCC CTGAGAAGGC ACTAAACCTG GAGTCAGACG CTGGGGTTTG AGCCGCAGCC 2580
CTACTGTTGT CTATGTGACT TTCGGAGCCT GTCCCTCTCT GAGCCTGTTT CCTCACCTGT 2640
GACATGGAGC AGAAGTTTCT ACATTGTCTG GCCTCAGGGG TCTAGGCAAA TCCTAGCAGT 2700
GACTGAATGG GAAGCCAAGG AAGTGGAAAT GGGACATGGC CCCTACTTCA AGTAGAATGA 2760
AACCCTTGTG ACCTGCTGTA AGCGGAAGGT TGTGTAGCAT TTCAATGGGG CAGAAAGAAA 2820
TCTGATACTG AAAAGCCTGT TTGGGAACCC TTGGACTAAA TGTCTCAGAA GCCACTCCAT 2880
TTTGAGCATT ACTTCTGTCT AATCTTAAAT GGTATGTGTG TGTGTGTACA TGTGTGTGCA 2940
TGTGTATGTG TGTGTGGGAA TGAAAAGTCA AAATGACAGC 2980
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