Tag | Content |
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EnhancerAtlas ID | HS037-02386 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr1:159892000-159893220 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr1:159892832-159892845 | AGCAGCTGTTTCT | + | 6.28 | Tcf12 | MA0521.1 | chr1:159892831-159892842 | CAGCAGCTGTT | - | 6.32 | YY1 | MA0095.2 | chr1:159892039-159892051 | CAACATGGCTGC | + | 6.14 |
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| Number of super-enhancer constituents: 46 | ID | Coordinate | Tissue/cell |
SE_02009 | chr1:159887204-159896462 | Aorta | SE_02391 | chr1:159891163-159896016 | Astrocytes | SE_09609 | chr1:159888811-159896163 | CD14 | SE_10233 | chr1:159889294-159896142 | CD19_Primary | SE_10984 | chr1:159884833-159896640 | CD20 | SE_11910 | chr1:159890466-159896330 | CD3 | SE_12862 | chr1:159890202-159896191 | CD34_Primary_RO01480 | SE_13325 | chr1:159887045-159896510 | CD34_Primary_RO01536 | SE_14052 | chr1:159890274-159896187 | CD34_Primary_RO01549 | SE_14513 | chr1:159890132-159896515 | CD4_Memory_Primary_7pool | SE_15769 | chr1:159891344-159896220 | CD4_Memory_Primary_8pool | SE_15949 | chr1:159891339-159896140 | CD4_Naive_Primary_7pool | SE_16460 | chr1:159890826-159896099 | CD4_Naive_Primary_8pool | SE_16913 | chr1:159890317-159896307 | CD4p_CD225int_CD127p_Tmem | SE_17500 | chr1:159889525-159896840 | CD4p_CD25-_CD45RAp_Naive | SE_17880 | chr1:159889025-159896700 | CD4p_CD25-_CD45ROp_Memory | SE_19597 | chr1:159888663-159896506 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20057 | chr1:159890184-159896627 | CD56 | SE_20849 | chr1:159889345-159896337 | CD8_Memory_7pool | SE_21561 | chr1:159891197-159896204 | CD8_Naive_7pool | SE_22506 | chr1:159889745-159896593 | CD8_primiary | SE_23567 | chr1:159891451-159896346 | Colon_Crypt_1 | SE_23939 | chr1:159892115-159896031 | Colon_Crypt_2 | SE_25013 | chr1:159890918-159896336 | Colon_Crypt_3 | SE_30108 | chr1:159891067-159896091 | Fetal_Muscle | SE_31985 | chr1:159891083-159896707 | Gastric | SE_34858 | chr1:159890807-159896516 | HeLa | SE_36438 | chr1:159891272-159896570 | HMEC | SE_38165 | chr1:159890321-159896029 | HUVEC | SE_40207 | chr1:159890880-159896228 | K562 | SE_41182 | chr1:159890906-159896421 | Left_Ventricle | SE_42315 | chr1:159887173-159896572 | Lung | SE_44957 | chr1:159891221-159895990 | NHLF | SE_47692 | chr1:159891560-159896059 | Pancreas | SE_48986 | chr1:159891201-159896458 | Right_Atrium | SE_49778 | chr1:159891574-159893172 | Right_Ventricle | SE_50509 | chr1:159888888-159896553 | Sigmoid_Colon | SE_52604 | chr1:159889149-159896485 | Small_Intestine | SE_53483 | chr1:159887801-159896526 | Spleen | SE_55434 | chr1:159890662-159896015 | Thymus | SE_58180 | chr1:159892507-159896090 | VACO_9m | SE_59359 | chr1:159879583-159907614 | Ly3 | SE_63031 | chr1:159879414-159896447 | Tonsil | SE_63399 | chr1:159883649-159916570 | NCI-H69 | SE_64771 | chr1:159890244-159896649 | NHEK | SE_65431 | chr1:159891110-159896368 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | AGAGGCTGTG TCTTGGGCCA GTCCCTCCCG TCCCGACTCC AACATGGCTG CTCCTTTTTA 60 CCCCAGCTTA TCAAGCTGCA CATTTCCGGC AGATCCTCCC CTAAATCAGT TATTTTTAAA 120 CCTCATTAAG AGCAACCCGC CCCCTCCACT TCCCCCAGCC CGAAAGCTGG GCCAGATAAA 180 TGTCAGTCTG GGCCCCGACC CACAGCGCCA GGCACACACA CCATCAGCTT GGGGAAGGCA 240 GGCGGGGTGG GGTGGCTGAG TTCTGAGGAG AAACCAAGAG AAGCATCCCT GCCCTTCCCA 300 GAGGCCACTC CACCATAGAA ACCTCTAACC TCTGATGCAC AGGGGAATGG CTGGAAGACA 360 GGTAGGAAGA GGAAGGGGCT AAGAGCTACT ACCACCAGTA AGCCCCCTTT CCGCAGCCCA 420 GTTCCAGACC TCTCTCCTGG GAGTGGCTGT GCTCAGGGCT GTTTCCAGGG ACCAAGTGGC 480 CTGAGGCTCG GGGATCACCA TGGCACAGGT AAAGAAAGGG CAGGAGAATG ATTAACCTAG 540 ACACTGGGGT TAAGAGCAGA GAGAAAGGCC TGAAGCCAGA CACTTCCAGT GCCCCCCAAC 600 CCCCCAAGGC AGGACAAACT TGGCCTCCCA GACCCACCAC TGGGTGGAAA GTGGATGCTG 660 AGGAACCCCC TCCACCGCCC AACGCTGGGG CCTGGACACA GCTGGCAGGG TCACGGCCTC 720 CAGCTGCAGT GTATCTGCTC CACTCTGGGG CCATTGCCCT CAAGCTCTGA GGTGCCAGAG 780 CCATAGGGCG GGGTCCTGAG AAGGGGCAGT TCCAACCAGG CCAGGCCTGG TCAGCAGCTG 840 TTTCTCTTCC CCACCCCCAC GGGCAGGCAG AAGCTGATGG GCTGCGGCTG CTGGAGCTGG 900 GAAGGCCCAC CCTAGGGACA CCCAGGGGAC CTGCCCCTGC CTTCCCTCAA ACATAAAGAA 960 AACAGTAAGC AAGTTGCCTA CCAGGGTGAG AAGAGATATG CCCAGCTGGA AGACAGGTGT 1020 GGGGGACCCC CAGAGCTGGG GACCCCAAAG GAAGGTGACA GCTGAACAAC CTGGGGGATG 1080 GACTGGCAGG GAGCAACCTA AACCCTAGCG CTACTGCAGC TGTGAGAACA ACCCTCACCC 1140 TCACCCTGGA GTTACAATAG GCGGGAAACG GGGAGGGGCC ACGCAAGGCA CTCGGCCCCA 1200 CCCAGACCCT GGGCTGGAAG 1220
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