Tag | Content |
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EnhancerAtlas ID | HS050-04417 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:159891040-159893220 |
SNPs | Number: 2 | 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: 2 | Chromosome | Start | End |
chr1 | 159892447 | 159892988 | chr1 | 159891200 | 159891400 |
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Enhancer Sequence | TAGATGTGAT TAAGATCTCG AAATGGGGAG ATTATCCTGC ATCATCTAAA TGAGCCCAGT 60 GTAATCACAA GGGCCTTACT AACTGAAAGT GGGAGATAGG TGAGTCAGAG TGGGAGAAGT 120 AACAACAACA ACAACAAAAT GGAAGTAGAA GTCAGAGTCA CACAGGGCCA TGAACCAAGC 180 AATGCAGGTG GCCTCCAGAA GCCAGAAAAG GGAAGGAAAT AGATTCACCC AAAAACCCCA 240 GAAGGAACAC AGCTCTGCCA ACACCTGTAT TTTAGCCAGT GAGACCCCTG TTGAGTCTGT 300 AGAACTGTAA GATGCTGTAT TTGTGTTGCT TTAAATCACT AAGCTTGTAG CAATTTGTTA 360 CAGCAGAAAT AGGAAACTAA TACAGGAGCC CTGGGTGATA TTTTTGGGGA AACCTGGAGA 420 AGAGAAGGCA AGACGGGGAA ATACACAGGA GGGTTTCTTT AACTTCGTTG GAGGAGCTTG 480 ATTAGCAAGA ACTGGGTGGT TTCCCGACCA ATGGCCTGAG TTGGCGGACC TCACTGTGGC 540 AGTGTGTTCC CACCACACTC ACCACCTGGG TCTGACACTC AGGGGCTGAG CAAGACCCGG 600 GCATGGTATG GATGCCAAGG GGAGCCAAGA ACCAAGAATG GGCCACAGTC CCCATTTTCT 660 GTCCCATCCC CACCCTGGTT TGGCTTTTCT CTCTTCTCCA AAACAGAGCT AGCTGTCAGG 720 CTGCTCACGA AAGGGGACCC CCAGGACAGG CATCTGCGTT CAAGGGGAAG AAAGAGAGCC 780 ACCCCTTCTA ACCACATCTG GCTCCAGGCC AGGTTGGCCT TCAGGGATGA AGTCACTCCA 840 GCTCCCCCTC TCCCACACAC CCAGGTTAAA CAATCCCGTC ACCCCCTCTC AATGGACCTT 900 GGGGCTCTGC GAAATACAAG GGGACCAGCC TGCCTCAAAC CCTCAACACC TCTCGGCCGC 960 AGAGGCTGTG TCTTGGGCCA GTCCCTCCCG TCCCGACTCC AACATGGCTG CTCCTTTTTA 1020 CCCCAGCTTA TCAAGCTGCA CATTTCCGGC AGATCCTCCC CTAAATCAGT TATTTTTAAA 1080 CCTCATTAAG AGCAACCCGC CCCCTCCACT TCCCCCAGCC CGAAAGCTGG GCCAGATAAA 1140 TGTCAGTCTG GGCCCCGACC CACAGCGCCA GGCACACACA CCATCAGCTT GGGGAAGGCA 1200 GGCGGGGTGG GGTGGCTGAG TTCTGAGGAG AAACCAAGAG AAGCATCCCT GCCCTTCCCA 1260 GAGGCCACTC CACCATAGAA ACCTCTAACC TCTGATGCAC AGGGGAATGG CTGGAAGACA 1320 GGTAGGAAGA GGAAGGGGCT AAGAGCTACT ACCACCAGTA AGCCCCCTTT CCGCAGCCCA 1380 GTTCCAGACC TCTCTCCTGG GAGTGGCTGT GCTCAGGGCT GTTTCCAGGG ACCAAGTGGC 1440 CTGAGGCTCG GGGATCACCA TGGCACAGGT AAAGAAAGGG CAGGAGAATG ATTAACCTAG 1500 ACACTGGGGT TAAGAGCAGA GAGAAAGGCC TGAAGCCAGA CACTTCCAGT GCCCCCCAAC 1560 CCCCCAAGGC AGGACAAACT TGGCCTCCCA GACCCACCAC TGGGTGGAAA GTGGATGCTG 1620 AGGAACCCCC TCCACCGCCC AACGCTGGGG CCTGGACACA GCTGGCAGGG TCACGGCCTC 1680 CAGCTGCAGT GTATCTGCTC CACTCTGGGG CCATTGCCCT CAAGCTCTGA GGTGCCAGAG 1740 CCATAGGGCG GGGTCCTGAG AAGGGGCAGT TCCAACCAGG CCAGGCCTGG TCAGCAGCTG 1800 TTTCTCTTCC CCACCCCCAC GGGCAGGCAG AAGCTGATGG GCTGCGGCTG CTGGAGCTGG 1860 GAAGGCCCAC CCTAGGGACA CCCAGGGGAC CTGCCCCTGC CTTCCCTCAA ACATAAAGAA 1920 AACAGTAAGC AAGTTGCCTA CCAGGGTGAG AAGAGATATG CCCAGCTGGA AGACAGGTGT 1980 GGGGGACCCC CAGAGCTGGG GACCCCAAAG GAAGGTGACA GCTGAACAAC CTGGGGGATG 2040 GACTGGCAGG GAGCAACCTA AACCCTAGCG CTACTGCAGC TGTGAGAACA ACCCTCACCC 2100 TCACCCTGGA GTTACAATAG GCGGGAAACG GGGAGGGGCC ACGCAAGGCA CTCGGCCCCA 2160 CCCAGACCCT GGGCTGGAAG 2180
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