| Tag | Content |
|---|
EnhancerAtlas ID | HS145-16995 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr3:46971830-46973680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr3:46972492-46972503 | AGGCACTCAAG | + | 6.14 | | Znf423 | MA0116.1 | chr3:46972788-46972803 | TCACCCCTAGGGTGC | - | 6.46 |
|
| | Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
| SE_00943 | chr3:46971562-46975179 | Adrenal_Gland | | SE_02008 | chr3:46971380-46975339 | Aorta | | SE_10127 | chr3:46964000-46982704 | CD14 | | SE_11155 | chr3:46963907-46992913 | CD20 | | SE_13638 | chr3:46971550-46974655 | CD34_Primary_RO01536 | | SE_14564 | chr3:46971566-46975300 | CD4_Memory_Primary_7pool | | SE_18708 | chr3:46972575-46975234 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20061 | chr3:46970016-46975395 | CD56 | | SE_22640 | chr3:46971928-46975052 | CD8_primiary | | SE_23114 | chr3:46971617-46975208 | Colon_Crypt_1 | | SE_23749 | chr3:46971711-46973448 | Colon_Crypt_2 | | SE_23749 | chr3:46973449-46975042 | Colon_Crypt_2 | | SE_26114 | chr3:46971685-46975312 | Duodenum_Smooth_Muscle | | SE_27403 | chr3:46970664-46979932 | Esophagus | | SE_28630 | chr3:46971492-46975383 | Fetal_Intestine_Large | | SE_30558 | chr3:46971654-46978550 | Fetal_Muscle | | SE_31407 | chr3:46970646-46975250 | Gastric | | SE_32585 | chr3:46966448-46975230 | GM12878 | | SE_38780 | chr3:46970749-46974865 | HUVEC | | SE_40617 | chr3:46970726-46975377 | Left_Ventricle | | SE_41619 | chr3:46971597-46975216 | LNCaP | | SE_42118 | chr3:46970032-46992962 | Lung | | SE_47478 | chr3:46971661-46973453 | Pancreas | | SE_48306 | chr3:46971528-46975218 | Psoas_Muscle | | SE_48684 | chr3:46971559-46975364 | Right_Atrium | | SE_49453 | chr3:46971538-46972807 | Right_Ventricle | | SE_49453 | chr3:46972817-46973621 | Right_Ventricle | | SE_50160 | chr3:46971539-46975248 | Sigmoid_Colon | | SE_52388 | chr3:46971545-46975260 | Small_Intestine | | SE_53507 | chr3:46970696-46975269 | Spleen | | 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 |
|
| | 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 |
| GH03I046924 | chr3 | 46966329 | 46982223 |
|
Enhancer Sequence | GCACCAGCAC CTCAGCTCTG CTGGTGGCCA GTCTCTGTGG CTTAGGGCCA GGCTGTCCCC 60
TAGCCAAAGG GAAGCAGAGA CCAAGCCATG CTTTTTTGGG GCTTTCTGCC CCCAGAGTCT 120
ATGGGAAGGA GGGCAGCCCA GAAAGCCCAA TGGCTTCTAA GACACTATCC TTTGCACCAA 180
ATGCCCTAGG CCACCCAAAG TCCACCCTAT ACCGGCAGCC AGTGTCTGGG TGGAGCTTTG 240
CTGTCTCTCC ACAGGAGCAG ACACATCAGC CACCTCAGTG CCTCCACTGG CCCTCCCTCT 300
GACTCAGGGA CCCCAGTGTC CCCAAAACAA GTCTAAGCTT CTTCACGTGG TCCTGGCCCC 360
ACAGCCTGCT CACCCCCTCA GCTACACACT TCCCCGTCCA TCACGCTTAA AGAGCCAGCT 420
CCAGGAGGTG GCCCTGTGGG CCCCTCCCAG TGTCCCTACT CACCCTGAGG CACAGTAACC 480
GCCCTTCTCC TGGGCCCCCT TTGCCCCACT TGCCTCTCTA CCCTCTCCAC AGCAGGCCCC 540
ACTCCATGCA CGTGGCCCTG TGTCGGCTGC ATGTCTGTCT TTCACAGCCT GCCCTAAATG 600
CACCAGGCAG CTCCAGGAGG GGCTCAGCAT ACATTGCCTC AAGCTGGATA AAGGAATTCA 660
GAAGGCACTC AAGAAAGAGC TTTATGGGTA GCCTGGGGCT CTCTGAGCCT TTCAATGACT 720
TGAGAAGACA TTTGGAAGCA AAGAAGTTGT GCCCAGCAGA GAGGGCAGGA ATGTGGCTGG 780
GCCGGGGCAG CCAACCCCTA AGCAACTTCT TTGTGGCAAA GCAACAGGGA ATGCCAAGTT 840
TGCATTCCAT AGAGTTTCCT TCTAAAATGG GTAGCTGACC TTTTCTATTT ACTTTACTCT 900
GCTTCAGGCC AGCTGCAGGA GCCCGGGACA TGGGCTGGCC AGGGAGGTTC AGGGGAAATC 960
ACCCCTAGGG TGCTTTTTCA CATGTGCCAA TGAGAGGAAG CAGGTGGAGA AAGTTGATGT 1020
TCTCTGTCAA GTATAGAACC AGAGTAGAGT TCTAGAATGG CGAAATGAAA GGAAGCTTTG 1080
AGATTATGAA TCTGATCCAA CCCCATCACT GGCAAACTGG CCTCAAAGCC TACACTGCTC 1140
ATGGGGGTTT CATGGCCCCT GGTCCACTTC ACTCACTCAT GCTACCAGGC TTATCCTTTG 1200
GGGCGCTAGC CTCCCTTCTC ATCCCTTATA TCTTGAGGCT ACTCCACATT CACCTGCTGC 1260
CCTGGGCCCC TGGAGGGAGG CAGAGAGGAT AAGGACAGGA CAGTCCCACA TGGCCTGTTC 1320
CCTGAGAACA AGGTCCTCCA CCTGGCCACC CTGGTCCCTC CTGGCCATAC AGGCCCCATC 1380
AAGGGCCAGA GAGAGAACTG CTGTGAGGCA CTCCTCCTAG TAACAGACCA CAGGGAAGGC 1440
CACGCCCAGG ATGCGCCTGC AGGCCTTGCA GAGGCCACCA CTGACCAGAG AGACTGGCAA 1500
CTTTGATCAA AGAACACTTT CATTTTTAAT ATTCAGAGTA CAGAGACACT GGAGCTCTGC 1560
CAGGAAAACA CACTCATGAC ACTCAGACAT GCCCCTAATA ATCCTCTGTT TGCTTTAGGC 1620
TCTGCACATA GAGACCTACC CCTTGTCCCC AATATAAATA ACAAGGCTTC AGTTGCTGCT 1680
GCCAGAGGCC AGACTCGACA GAAGCATGAA AATGAGGGGA GAGGCAACTA CCCCAAATGA 1740
GGTACACAAC TGCTCTAGAG GCTGATCTGG TCTTTCTTTC AAGGGCCATT AAAATGTTCA 1800
AACTCCCTGA CCCGGTAACC CTGCTCTGGG GAAATTATTC CATAGAAATA 1850
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