| Tag | Content |
|---|
EnhancerAtlas ID | HS145-16996 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr3:46983160-46985680 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr3:46984413-46984424 | GCAGGGTGTGG | - | 6.62 | | NKX2-3 | MA0672.1 | chr3:46985552-46985562 | ACCACTTGAA | + | 6.02 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_00943 | chr3:46983643-46987096 | Adrenal_Gland | | SE_11155 | chr3:46963907-46992913 | CD20 | | SE_14564 | chr3:46984749-46992585 | CD4_Memory_Primary_7pool | | SE_20061 | chr3:46985017-46993140 | CD56 | | SE_23114 | chr3:46983008-46987127 | Colon_Crypt_1 | | SE_23749 | chr3:46983035-46987037 | Colon_Crypt_2 | | SE_26114 | chr3:46983078-46991394 | Duodenum_Smooth_Muscle | | SE_27142 | chr3:46983018-46992857 | Esophagus | | SE_28145 | chr3:46982939-46992085 | Fetal_Intestine | | SE_28630 | chr3:46982992-46992260 | Fetal_Intestine_Large | | SE_30558 | chr3:46984380-46986112 | Fetal_Muscle | | SE_31407 | chr3:46975429-46987226 | Gastric | | SE_38780 | chr3:46984005-46987196 | HUVEC | | SE_40617 | chr3:46975387-46993135 | Left_Ventricle | | SE_42118 | chr3:46970032-46992962 | Lung | | SE_47478 | chr3:46983535-46987108 | Pancreas | | SE_48306 | chr3:46984091-46987099 | Psoas_Muscle | | SE_48684 | chr3:46982967-46987123 | Right_Atrium | | SE_49453 | chr3:46983064-46985439 | Right_Ventricle | | SE_50160 | chr3:46983018-46987192 | Sigmoid_Colon | | SE_52388 | chr3:46983042-46987272 | Small_Intestine | | SE_58746 | chr3:46966845-47032612 | Ly1 | | SE_59412 | chr3:46966960-46998383 | Ly3 | | SE_59747 | chr3:46966600-47033537 | Ly4 | | SE_60850 | chr3:46965041-47030117 | DHL6 | | SE_62445 | chr3:46966331-47033109 | Tonsil | | SE_64772 | chr3:46984018-46985866 | NHEK | | SE_65471 | chr3:46977753-46993036 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr3 | 46983444 | 46983555 | | chr3 | 46983650 | 46983795 | | chr3 | 46983837 | 46983956 | | chr3 | 46984267 | 46984496 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I046941 | chr3 | 46983048 | 46992889 |
|
Enhancer Sequence | TGAGAAATGC AGCCACTTGG TGCCATGGAG GGGCCATGCT GGCAGGCCAG CAGTCACCTT 60
CATGGGTCTA GACAGAACCA CCTGCTAAGC TAGGAAAGAC TGGGGAAAGA AGTTACCAGC 120
AACCAGGGCA GGATGAGAGC TCAGGCCTCC TGAGACACCT TTCAGGCCAG AGTCCTCTCC 180
AGAAATACCT ATTTGATTCG CTTTAGAAGT AACATGAACT AGGACCAGGC TTGCAACAAG 240
ATTCACTGCC TAGGCCTATG CTATATTCAG GGAGACAGAG GCAAGGGGAA TTAGTCTGAA 300
GTTTCCATGA AAATTTTCTT AATCTGGTTC TTTTGACTTC CCACCAACTG CACCTCTTTT 360
TGAAGTCTAC AGAGTCATGT TCATCTCAAC CTTGACATGT TATGCTTGTT CTCAGGTGCA 420
CTGGGGGCCA CAACAGAAGG AAACTGCCAT ACTGCTTCCA CCTGAAGCAG AAAATGTCTT 480
CCTGGACTTT ATCCTTTATT ATGTGATTAC CTCTGTTAGG TCAGCCTGCC TGTGGACAAA 540
CTGACGCAGG GCGTGTGTGC ACATGCACAA ATTCGTGTGA CCACACCTGG GGCCCAGGGC 600
ATGGACTGAG AGGCCCCAAG ACAGAGCTGT CGTGGGTCTC CCTGCATGCC AGGGTTGGCA 660
CTCCAGAAGG TGACAATGCT CACTTCACTA TGGCAGCGTC CTGCCTTTGA CTCTCGCAGA 720
GCAGTGTTCT AAGAGAGATC TGTGAGCTCC TTCCATTGGG AGCCTGCTCT GGTGGACACA 780
GAATGCGCTG GAGCCTGCAT ATAAATTATA AGTAAAACAG CTACTTGAAC TACCTTTCCT 840
AGACATTTAT TTATGCCATT GACAACTGCC TTCCTAAGAA TGGTATCTGC TTTATGTGGA 900
GACTGCAGGC ATCAACCAGA CCCTGCCATT CCTTGGCCAC ACAACCTCCG GGGAGCAGAC 960
TACCAAAACC AGGTCGGAGG CCTGGCCCAG AGAAAGGCTT CTGTCATGAG AACAGATCAA 1020
CATGCCCCCC ACCCCAACTC AGGGCAGCTC ATCTCATGGC AACGAGGCAG CGAGAACAAA 1080
ATAACTGACC AAGTGACAGC AGCTACACGA GAGAGGTCAA CATGGAACGT GGTTCTTGGG 1140
CGATGGGTGA GAGGTTTCCT ACTGAGAGAT GGGCTGGGCA GAATTGGGTG ATACAGCATA 1200
GGGGGAGAGA AGTGGGAAGG GCATTCCCGG TGGGAAGCAG AGCTTGAACA AAGGCAGGGT 1260
GTGGTCTGAA GAGCATGCAG GTGACTGGGG TTGGGGGAGG GGGTGACAAT GATTGCCAGG 1320
TAAGACAGTC AAGGCAGGCA ATGGCCGAAC ACAGAGGGCT CTGGCCGGTG TTCTTAAGCA 1380
ATGGAGAAAC CGAGGAGAGA CTGGAGAGAG TTCACTGACC TCTGCTGGGG AAGGCAGGCC 1440
CTGGGGTGGA CAGGCAGATG CTTGGTGATG GCCAAAGAGG GAAGGGAGAA CAGAGTATAA 1500
ATGCTTCACT GAGAAACAAG TCAGGATTCT CCAAATGGCT CCCAGGGCTG CTGGGACCTG 1560
GACGGGGCTT CCACAAGGGC CCTGCTGACA CATGCAGCCC TCCCTGACTA AAGACTAGCC 1620
GATGAAGCAA GCCAGAGCCT GCAAATTCTA GCAAAAAATT CCTTCCCAAC TCCCAACCAG 1680
CGGACACCCT GAAGGCTACT CCCTGCAGTG CCTACCTCAG GGGAAGGAGC GGCAGACACC 1740
TGCCCTGGGT AAGGGCAGAG AAGGAAAAGC AGAAAGGGCT CTTCTTTCCC CACACTGGGC 1800
TAGTGGGGCA AGACCCCCAG CCACAAAGAC GACTCCTTTC CACAGGGGTT CTGTTAACCC 1860
GAACCACCTG GCAGAAGTAG GTGGGGACTA CGGGAAAGTG TCCAGCCTTT GGGAGGAGTG 1920
CTTTGCAAAT ACCATGCCCT TTCTCGGCTC TCAAGCAAGG TCAAACAGCT GTCACCACCC 1980
TCCTGGAGCC CCAGAGACAT TCAAGTGCCT CAGCAAAGGC CAAGTTATTC ATTAATAAAT 2040
GAGAAAACAC CCAACTATCT AAATGACTTT TAAAAATGCC CAGCAATCTG GTGGGTGGGG 2100
GGCAGCACTA GCTCTGCAGA CAGCATGAGG TTAAAAATGA CCCCAGCCTG GGATGCTGTG 2160
CAAAGAGCAG GGGCTCAAAA AAGATAAAGA TCCACATCTG TGGCAGGAGC AGGTGAACAA 2220
ATGAACAGGC CACACAAGTG GGGGAGATAA GGTGTACCTC AGCCTTCCTG ACAAAGAGTG 2280
ATTCATAAAT AGGACAATGG GCATTCACGG GAAGGAAAAT CGCTTTTGGT GACACTGGCC 2340
TGAATCACAA GATAAGGCCC TTTGCTGCCC GGGATAGTGG AGGGAAGCGC AGACCACTTG 2400
AAGCTCACCC CTACCTGAGA GACTCAAAGA GCCTCAGACC TGGAGGGCTC GCAGGATCAC 2460
CCATTCTAGG TCCTCAGTTT AAGCCATGGG AAAACCTGGG AAATGGCAGT CAGGGAAAAG 2520
|
