| Tag | Content |
|---|
EnhancerAtlas ID | HS129-25184 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr3:46987350-46989300 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr3:46987600-46987621 | GGAGGAGGGAGGAAGAAGAGA | + | 7.09 |
|
| | 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_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 | chr3:46987353-46987816 | Pancreas | | SE_47478 | chr3:46987822-46991381 | Pancreas | | SE_48306 | chr3:46987919-46991489 | Psoas_Muscle | | SE_48684 | chr3:46987782-46991986 | Right_Atrium | | SE_49453 | chr3:46987335-46987794 | Right_Ventricle | | SE_49453 | chr3:46987803-46989682 | 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: 2 | Chromosome | Start | End |
| chr3 | 46987931 | 46988653 | | chr3 | 46988775 | 46989017 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I046941 | chr3 | 46983048 | 46992889 |
|
Enhancer Sequence | TGTGTCATTT TTCTTTATCA GACCAGCTAG AGGTTTATCA ATTTTGGGAC GTGCCTCCAT 60
CTCATCTCCT CAGACTCGGT GTTTCAACAA TGGCTTTGCT CCTCAGTCAC CTCTCTCTGG 120
AAGGATCCCT CAATGGATGA GTACACCTGC CTCTGGATGG CACATGAAGC GTGGGGGCAG 180
AATCAATCCA CATTGCTGTC TGAATGTAGT ACCACTGCTA GAAGCAGGTC AATCAACAAC 240
CAGGCCTACA GGAGGAGGGA GGAAGAAGAG AGGCTGCTCT ATGTCCTCCT CTTGCCCCTT 300
CCCACCCACA GTAAGATGAA GATCTCTTTC CTTGCACCCC TCAGTCTCCT TTGTGGGCCA 360
GGTCTACCTT GGGCACAAAG ATAAAGTAAG AACCCTATCG TCAAGAATCT CAAGTCTACT 420
CAAAGGATCA GACTTAGAAA ATGTAACTCT GTGCCATGAG TAGTAAGGAA AGCTTTACTA 480
AATATCTTGT ACACTTAGGG AATTAGCAAG GGATAGGTGT TGTCGGGGAA GGAAGTAATG 540
CTTAAACTCA ATTCTAAATG TCCACTGGGG GATTATGAGG CAGCTAAAGA AGGCAGAGCA 600
TTCCTGGGAG TGGTAACTGC CTACAAAGAC ATGAGAGCGG AGCAAGAGCA CTGTCACAGC 660
CTGCAGAGCA GGCCCACATG GCTGGCCCAG CCTCACCTGA TGCTGTCAGG GGCAGGGCTC 720
ACAGGGCATT CCTCCAGCAC CGTGGGAGGG CTGAGCCCAG CATGAGGGCC GACACCCTGA 780
ACGGGCACTG TGGTAGCCTA CAAGATGTGT CATGGGAGGA ACGGGGAAGA CCAGAAGTCA 840
GGTGAGATCC TCCACTCCCA GCCTGGACCT GCCCCAGCCT GCTGCTGTCT GTGTGTCTGT 900
GTTTGGGAGG GGGGTTAAAG TTAAAATGAG GGCTGGGAAC TGTCACTGGG GGCGGGTGTG 960
CCGAAGCAGG AGGACTTGAG TTCAGGGGAT GAGGAATAAG CCCCTCCCTC TCCCTAAGAC 1020
TTCCCAAGGA CTCAAACTTT TAGGAGCTGC TGACTAGAGC TCTCCCTTCC AGAAGGAAAT 1080
AAGAGAAGCA GGAAAGGGTT AAGAGAGAGA CATTCAACTT CTCATCTAGG GTCTTCCCAC 1140
CCTTCTTTAG CTTCCTGAAG AAGCTAGAGA CTCACCAGGA ACTCATGGGT ACAGAAACAC 1200
TTTCCAATCC CCAGGTGATA TGCCCCATTA GCTCTGAGTA CGCCTGCTAT AATGTCCATG 1260
GGAAACTGCC CTCTGTTCAA AAGTTAAAGA GAAAATAAGA CCTCGAAATC CTAGCCCCCT 1320
AAGAAGAGGC CAAACTGGCC CCACTTTGAG CCTTTCCAGT TCTGATTTGG GCCCAGGGTG 1380
GGGAAAAAAG CAAAAGAGAT GGGCACATAG TGCCTGAAGG TGACAGGAAG AGACAGACAA 1440
TGCTGGGGCA AACTTGGCAG GCTCCCCAGT GTCACCTTGT GCCCATCCTC AGGGCCACTG 1500
CAGCCCCATG CCGGGGTGGA GGGACTTCCT GTCGGGTGCT GCCGTGGTGG GAGCTGTGTT 1560
CCAAGGGCAC TTAGCGGGTA GGGCAGTCAC CCGGAGTCTG ACTCACCCTG AAGATGGAGT 1620
GATAAGAAGT GAGCTGAACA CCACCATGCC TGGGACCAGA AACTGCACAG ATCTCTACTG 1680
CCCAGAGACT GGCAGGGGGA AAGGGGGAGA GACTCTGCTT CTCCTGGGCA GGCTGAGATC 1740
TCGTCAGGCT GCAGAGCTCC TCACTCTGGG TCCCCTGCAC TCAATGTGCT GCTAGGATGA 1800
CTTGGTCCGA GTATCCACTC TATCTGCTGA CCAGACCAAG AGTTCCTAGA GGGCAGACGT 1860
TTGTTGTACC AGTTTGCACC CACAGGCCTG ACACCAACTA CAGCAGGCAC AGCACTGTGG 1920
TAGAGGAGTG CACAGGAGCG GGGAAATCCC 1950
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