Tag | Content |
---|
EnhancerAtlas ID | HS095-02174 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:159891470-159893220 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGACGGGGAA ATACACAGGA GGGTTTCTTT AACTTCGTTG GAGGAGCTTG ATTAGCAAGA 60 ACTGGGTGGT TTCCCGACCA ATGGCCTGAG TTGGCGGACC TCACTGTGGC AGTGTGTTCC 120 CACCACACTC ACCACCTGGG TCTGACACTC AGGGGCTGAG CAAGACCCGG GCATGGTATG 180 GATGCCAAGG GGAGCCAAGA ACCAAGAATG GGCCACAGTC CCCATTTTCT GTCCCATCCC 240 CACCCTGGTT TGGCTTTTCT CTCTTCTCCA AAACAGAGCT AGCTGTCAGG CTGCTCACGA 300 AAGGGGACCC CCAGGACAGG CATCTGCGTT CAAGGGGAAG AAAGAGAGCC ACCCCTTCTA 360 ACCACATCTG GCTCCAGGCC AGGTTGGCCT TCAGGGATGA AGTCACTCCA GCTCCCCCTC 420 TCCCACACAC CCAGGTTAAA CAATCCCGTC ACCCCCTCTC AATGGACCTT GGGGCTCTGC 480 GAAATACAAG GGGACCAGCC TGCCTCAAAC CCTCAACACC TCTCGGCCGC AGAGGCTGTG 540 TCTTGGGCCA GTCCCTCCCG TCCCGACTCC AACATGGCTG CTCCTTTTTA CCCCAGCTTA 600 TCAAGCTGCA CATTTCCGGC AGATCCTCCC CTAAATCAGT TATTTTTAAA CCTCATTAAG 660 AGCAACCCGC CCCCTCCACT TCCCCCAGCC CGAAAGCTGG GCCAGATAAA TGTCAGTCTG 720 GGCCCCGACC CACAGCGCCA GGCACACACA CCATCAGCTT GGGGAAGGCA GGCGGGGTGG 780 GGTGGCTGAG TTCTGAGGAG AAACCAAGAG AAGCATCCCT GCCCTTCCCA GAGGCCACTC 840 CACCATAGAA ACCTCTAACC TCTGATGCAC AGGGGAATGG CTGGAAGACA GGTAGGAAGA 900 GGAAGGGGCT AAGAGCTACT ACCACCAGTA AGCCCCCTTT CCGCAGCCCA GTTCCAGACC 960 TCTCTCCTGG GAGTGGCTGT GCTCAGGGCT GTTTCCAGGG ACCAAGTGGC CTGAGGCTCG 1020 GGGATCACCA TGGCACAGGT AAAGAAAGGG CAGGAGAATG ATTAACCTAG ACACTGGGGT 1080 TAAGAGCAGA GAGAAAGGCC TGAAGCCAGA CACTTCCAGT GCCCCCCAAC CCCCCAAGGC 1140 AGGACAAACT TGGCCTCCCA GACCCACCAC TGGGTGGAAA GTGGATGCTG AGGAACCCCC 1200 TCCACCGCCC AACGCTGGGG CCTGGACACA GCTGGCAGGG TCACGGCCTC CAGCTGCAGT 1260 GTATCTGCTC CACTCTGGGG CCATTGCCCT CAAGCTCTGA GGTGCCAGAG CCATAGGGCG 1320 GGGTCCTGAG AAGGGGCAGT TCCAACCAGG CCAGGCCTGG TCAGCAGCTG TTTCTCTTCC 1380 CCACCCCCAC GGGCAGGCAG AAGCTGATGG GCTGCGGCTG CTGGAGCTGG GAAGGCCCAC 1440 CCTAGGGACA CCCAGGGGAC CTGCCCCTGC CTTCCCTCAA ACATAAAGAA AACAGTAAGC 1500 AAGTTGCCTA CCAGGGTGAG AAGAGATATG CCCAGCTGGA AGACAGGTGT GGGGGACCCC 1560 CAGAGCTGGG GACCCCAAAG GAAGGTGACA GCTGAACAAC CTGGGGGATG GACTGGCAGG 1620 GAGCAACCTA AACCCTAGCG CTACTGCAGC TGTGAGAACA ACCCTCACCC TCACCCTGGA 1680 GTTACAATAG GCGGGAAACG GGGAGGGGCC ACGCAAGGCA CTCGGCCCCA CCCAGACCCT 1740 GGGCTGGAAG 1750
|