| Tag | Content |
|---|
EnhancerAtlas ID | HS109-15310 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr3:46988700-46990330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr3:46989860-46989871 | AGAGATAAGGA | - | 6.02 | | NR2F1 | MA0017.2 | chr3:46989541-46989554 | CAGAGGTCATGGG | + | 6.22 |
|
| | Number of super-enhancer constituents: 37 | ID | Coordinate | Tissue/cell |
| SE_00943 | chr3:46987333-46991985 | Adrenal_Gland | | SE_02008 | chr3:46987772-46990525 | Aorta | | SE_11155 | chr3:46963907-46992913 | CD20 | | SE_13638 | chr3:46988105-46991652 | CD34_Primary_RO01536 | | SE_14564 | chr3:46984749-46992585 | CD4_Memory_Primary_7pool | | SE_16650 | chr3:46987830-46991302 | CD4_Naive_Primary_8pool | | SE_18708 | chr3:46986099-46991562 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20061 | chr3:46985017-46993140 | CD56 | | SE_22640 | chr3:46985615-46991406 | CD8_primiary | | SE_23114 | chr3:46987260-46991352 | Colon_Crypt_1 | | SE_23749 | chr3:46987346-46991294 | 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 | chr3:46988988-46991255 | Fetal_Muscle | | SE_31407 | chr3:46987243-46992180 | Gastric | | SE_32585 | chr3:46989343-46991413 | GM12878 | | SE_38780 | chr3:46987824-46991550 | HUVEC | | SE_40617 | chr3:46975387-46993135 | Left_Ventricle | | SE_41619 | chr3:46988621-46991305 | LNCaP | | SE_42118 | chr3:46970032-46992962 | Lung | | SE_47478 | chr3:46987822-46991381 | Pancreas | | SE_48306 | chr3:46987919-46991489 | Psoas_Muscle | | SE_48684 | chr3:46987782-46991986 | Right_Atrium | | SE_49453 | chr3:46987803-46989682 | Right_Ventricle | | SE_49453 | chr3:46989698-46991296 | Right_Ventricle | | SE_50160 | chr3:46987309-46992159 | Sigmoid_Colon | | SE_52388 | chr3:46987277-46992190 | Small_Intestine | | SE_53507 | chr3:46987802-46992203 | 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 | | SE_64772 | chr3:46987179-46991025 | NHEK | | SE_65471 | chr3:46977753-46993036 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr3 | 46989533 | 46989702 | | chr3 | 46988775 | 46989017 | | chr3 | 46989736 | 46990203 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I046941 | chr3 | 46983048 | 46992889 |
|
Enhancer Sequence | CCTTTCCAGT TCTGATTTGG GCCCAGGGTG GGGAAAAAAG CAAAAGAGAT GGGCACATAG 60
TGCCTGAAGG TGACAGGAAG AGACAGACAA TGCTGGGGCA AACTTGGCAG GCTCCCCAGT 120
GTCACCTTGT GCCCATCCTC AGGGCCACTG CAGCCCCATG CCGGGGTGGA GGGACTTCCT 180
GTCGGGTGCT GCCGTGGTGG GAGCTGTGTT CCAAGGGCAC TTAGCGGGTA GGGCAGTCAC 240
CCGGAGTCTG ACTCACCCTG AAGATGGAGT GATAAGAAGT GAGCTGAACA CCACCATGCC 300
TGGGACCAGA AACTGCACAG ATCTCTACTG CCCAGAGACT GGCAGGGGGA AAGGGGGAGA 360
GACTCTGCTT CTCCTGGGCA GGCTGAGATC TCGTCAGGCT GCAGAGCTCC TCACTCTGGG 420
TCCCCTGCAC TCAATGTGCT GCTAGGATGA CTTGGTCCGA GTATCCACTC TATCTGCTGA 480
CCAGACCAAG AGTTCCTAGA GGGCAGACGT TTGTTGTACC AGTTTGCACC CACAGGCCTG 540
ACACCAACTA CAGCAGGCAC AGCACTGTGG TAGAGGAGTG CACAGGAGCG GGGAAATCCC 600
AGCTCCATTT CATCTTGGCT GTGTGACCTT GGGCAAGTTA TATGACCTGT CTGGCCTCAG 660
TTTCCTCATC TACAAAAATG AGGATAATCA TACTGACATC ATATCACCAT TACAAGGAAA 720
TGATGAAGGA GAAAAGCCTG CAGCTTAGGG AGCCTGAAGA ACAGGGAGAA TCAGGCCAGG 780
GCAGGAAGGA AAGGGCTGCA GAAAAGCCAG CGGGGCACAG GCCCAGAACG GTGTGCCTCT 840
GCAGAGGTCA TGGGAAGCTC CCATGCCCAT CATCCTTATC AGATGTTCTC AGCAATCCTG 900
TAAGCAGACA GGGCAGTGTT GTAATACCTG CTTCACCAAG ACATTAGGAG ATGACGTCAG 960
ATGATCTGTG CAGTGTAGAC AGATCTGATT CCCCATTCAG TGCTTCACCA AGAGTCAGCA 1020
GGAACAGGTG GTGACTACCA TCCAAGAGGC TGGGATTAGC TAAGAGCCAC TGCTCTCCTG 1080
TGGGTTCATG TGTTCCCTAA AGGCTTCTGA GCAGAGCAAG AACAAAGCGC TGAGCGGGAG 1140
GCTGGGAGAA CAGCGAGGCT AGAGATAAGG ACTGGAGATA AGGACGGGAA CTAGGTCAAC 1200
AGCGGTGGAC TAGAACAAGG AGGTGCCTCA ACGCTGTGGG GAGACAGGGA GGAGCAGAAA 1260
CAACTGAGGT TCTGCTGGTG ACTCACTGGG GGAAGGAAGG CGCCTTTGAC AAAAAGGTGG 1320
TGGCACTTAG GGGACAAAGA GAAAGGGTGT GGCAGCCTTC AGGCATTCTA ACGGTGAGGC 1380
TTGACACCCA AGGCCTGACG AAGGTTGGTG CCAAGGGATA GCACCTGTCA AGGTGCCCTC 1440
AGCGGTGGAA AGGAGGGCCC GCTCCACTCA GAAGAGAGGC ACGCTGGGCC CCACCATCCA 1500
TATGGCACCT CAAGGGCCAG GCCACGGCAT GCCTAGTGCA GCTCCTCGCC AGGCCCGTCA 1560
CACGGCCCTG CCCAGATATC CTCCATGTGT CTGTCAGGAG TGTGGGGAGC CAGCCCAAGT 1620
CAACTCTGAT 1630
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