| Tag | Content |
|---|
EnhancerAtlas ID | HS176-26071 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr3:46987960-46990500 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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: 4 | Chromosome | Start | End |
| chr3 | 46989533 | 46989702 | | chr3 | 46988775 | 46989017 | | chr3 | 46988686 | 46990431 | | chr3 | 46989736 | 46990203 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I046941 | chr3 | 46983048 | 46992889 |
|
Enhancer Sequence | TGGTAACTGC CTACAAAGAC ATGAGAGCGG AGCAAGAGCA CTGTCACAGC CTGCAGAGCA 60
GGCCCACATG GCTGGCCCAG CCTCACCTGA TGCTGTCAGG GGCAGGGCTC ACAGGGCATT 120
CCTCCAGCAC CGTGGGAGGG CTGAGCCCAG CATGAGGGCC GACACCCTGA ACGGGCACTG 180
TGGTAGCCTA CAAGATGTGT CATGGGAGGA ACGGGGAAGA CCAGAAGTCA GGTGAGATCC 240
TCCACTCCCA GCCTGGACCT GCCCCAGCCT GCTGCTGTCT GTGTGTCTGT GTTTGGGAGG 300
GGGGTTAAAG TTAAAATGAG GGCTGGGAAC TGTCACTGGG GGCGGGTGTG CCGAAGCAGG 360
AGGACTTGAG TTCAGGGGAT GAGGAATAAG CCCCTCCCTC TCCCTAAGAC TTCCCAAGGA 420
CTCAAACTTT TAGGAGCTGC TGACTAGAGC TCTCCCTTCC AGAAGGAAAT AAGAGAAGCA 480
GGAAAGGGTT AAGAGAGAGA CATTCAACTT CTCATCTAGG GTCTTCCCAC CCTTCTTTAG 540
CTTCCTGAAG AAGCTAGAGA CTCACCAGGA ACTCATGGGT ACAGAAACAC TTTCCAATCC 600
CCAGGTGATA TGCCCCATTA GCTCTGAGTA CGCCTGCTAT AATGTCCATG GGAAACTGCC 660
CTCTGTTCAA AAGTTAAAGA GAAAATAAGA CCTCGAAATC CTAGCCCCCT AAGAAGAGGC 720
CAAACTGGCC CCACTTTGAG CCTTTCCAGT TCTGATTTGG GCCCAGGGTG GGGAAAAAAG 780
CAAAAGAGAT GGGCACATAG TGCCTGAAGG TGACAGGAAG AGACAGACAA TGCTGGGGCA 840
AACTTGGCAG GCTCCCCAGT GTCACCTTGT GCCCATCCTC AGGGCCACTG CAGCCCCATG 900
CCGGGGTGGA GGGACTTCCT GTCGGGTGCT GCCGTGGTGG GAGCTGTGTT CCAAGGGCAC 960
TTAGCGGGTA GGGCAGTCAC CCGGAGTCTG ACTCACCCTG AAGATGGAGT GATAAGAAGT 1020
GAGCTGAACA CCACCATGCC TGGGACCAGA AACTGCACAG ATCTCTACTG CCCAGAGACT 1080
GGCAGGGGGA AAGGGGGAGA GACTCTGCTT CTCCTGGGCA GGCTGAGATC TCGTCAGGCT 1140
GCAGAGCTCC TCACTCTGGG TCCCCTGCAC TCAATGTGCT GCTAGGATGA CTTGGTCCGA 1200
GTATCCACTC TATCTGCTGA CCAGACCAAG AGTTCCTAGA GGGCAGACGT TTGTTGTACC 1260
AGTTTGCACC CACAGGCCTG ACACCAACTA CAGCAGGCAC AGCACTGTGG TAGAGGAGTG 1320
CACAGGAGCG GGGAAATCCC AGCTCCATTT CATCTTGGCT GTGTGACCTT GGGCAAGTTA 1380
TATGACCTGT CTGGCCTCAG TTTCCTCATC TACAAAAATG AGGATAATCA TACTGACATC 1440
ATATCACCAT TACAAGGAAA TGATGAAGGA GAAAAGCCTG CAGCTTAGGG AGCCTGAAGA 1500
ACAGGGAGAA TCAGGCCAGG GCAGGAAGGA AAGGGCTGCA GAAAAGCCAG CGGGGCACAG 1560
GCCCAGAACG GTGTGCCTCT GCAGAGGTCA TGGGAAGCTC CCATGCCCAT CATCCTTATC 1620
AGATGTTCTC AGCAATCCTG TAAGCAGACA GGGCAGTGTT GTAATACCTG CTTCACCAAG 1680
ACATTAGGAG ATGACGTCAG ATGATCTGTG CAGTGTAGAC AGATCTGATT CCCCATTCAG 1740
TGCTTCACCA AGAGTCAGCA GGAACAGGTG GTGACTACCA TCCAAGAGGC TGGGATTAGC 1800
TAAGAGCCAC TGCTCTCCTG TGGGTTCATG TGTTCCCTAA AGGCTTCTGA GCAGAGCAAG 1860
AACAAAGCGC TGAGCGGGAG GCTGGGAGAA CAGCGAGGCT AGAGATAAGG ACTGGAGATA 1920
AGGACGGGAA CTAGGTCAAC AGCGGTGGAC TAGAACAAGG AGGTGCCTCA ACGCTGTGGG 1980
GAGACAGGGA GGAGCAGAAA CAACTGAGGT TCTGCTGGTG ACTCACTGGG GGAAGGAAGG 2040
CGCCTTTGAC AAAAAGGTGG TGGCACTTAG GGGACAAAGA GAAAGGGTGT GGCAGCCTTC 2100
AGGCATTCTA ACGGTGAGGC TTGACACCCA AGGCCTGACG AAGGTTGGTG CCAAGGGATA 2160
GCACCTGTCA AGGTGCCCTC AGCGGTGGAA AGGAGGGCCC GCTCCACTCA GAAGAGAGGC 2220
ACGCTGGGCC CCACCATCCA TATGGCACCT CAAGGGCCAG GCCACGGCAT GCCTAGTGCA 2280
GCTCCTCGCC AGGCCCGTCA CACGGCCCTG CCCAGATATC CTCCATGTGT CTGTCAGGAG 2340
TGTGGGGAGC CAGCCCAAGT CAACTCTGAT CCTATTCTTG CTGCAAGTGC TCAAGGGAGG 2400
CACTACAGAG CTCCTCCAGC AGACTTTATC AGTCGACAAA TACTGACTGG CTCCCCTGTG 2460
GTACTCCATG CTGTACTCAG ATACTCCATG CTGGGTACTG AGGAGGAAGA GGAACGAGTA 2520
GGCACCTAGT GCCCACAGAG 2540
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