Tag | Content |
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EnhancerAtlas ID | HS115-00346 |
Organism | Homo sapiens |
Tissue/cell | Kidney_cortex |
Coordinate | chr1:159891390-159893220 |
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: 1 | Chromosome | Start | End |
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Enhancer Sequence | CAATTTGTTA CAGCAGAAAT AGGAAACTAA TACAGGAGCC CTGGGTGATA TTTTTGGGGA 60 AACCTGGAGA AGAGAAGGCA AGACGGGGAA ATACACAGGA GGGTTTCTTT AACTTCGTTG 120 GAGGAGCTTG ATTAGCAAGA ACTGGGTGGT TTCCCGACCA ATGGCCTGAG TTGGCGGACC 180 TCACTGTGGC AGTGTGTTCC CACCACACTC ACCACCTGGG TCTGACACTC AGGGGCTGAG 240 CAAGACCCGG GCATGGTATG GATGCCAAGG GGAGCCAAGA ACCAAGAATG GGCCACAGTC 300 CCCATTTTCT GTCCCATCCC CACCCTGGTT TGGCTTTTCT CTCTTCTCCA AAACAGAGCT 360 AGCTGTCAGG CTGCTCACGA AAGGGGACCC CCAGGACAGG CATCTGCGTT CAAGGGGAAG 420 AAAGAGAGCC ACCCCTTCTA ACCACATCTG GCTCCAGGCC AGGTTGGCCT TCAGGGATGA 480 AGTCACTCCA GCTCCCCCTC TCCCACACAC CCAGGTTAAA CAATCCCGTC ACCCCCTCTC 540 AATGGACCTT GGGGCTCTGC GAAATACAAG GGGACCAGCC TGCCTCAAAC CCTCAACACC 600 TCTCGGCCGC AGAGGCTGTG TCTTGGGCCA GTCCCTCCCG TCCCGACTCC AACATGGCTG 660 CTCCTTTTTA CCCCAGCTTA TCAAGCTGCA CATTTCCGGC AGATCCTCCC CTAAATCAGT 720 TATTTTTAAA CCTCATTAAG AGCAACCCGC CCCCTCCACT TCCCCCAGCC CGAAAGCTGG 780 GCCAGATAAA TGTCAGTCTG GGCCCCGACC CACAGCGCCA GGCACACACA CCATCAGCTT 840 GGGGAAGGCA GGCGGGGTGG GGTGGCTGAG TTCTGAGGAG AAACCAAGAG AAGCATCCCT 900 GCCCTTCCCA GAGGCCACTC CACCATAGAA ACCTCTAACC TCTGATGCAC AGGGGAATGG 960 CTGGAAGACA GGTAGGAAGA GGAAGGGGCT AAGAGCTACT ACCACCAGTA AGCCCCCTTT 1020 CCGCAGCCCA GTTCCAGACC TCTCTCCTGG GAGTGGCTGT GCTCAGGGCT GTTTCCAGGG 1080 ACCAAGTGGC CTGAGGCTCG GGGATCACCA TGGCACAGGT AAAGAAAGGG CAGGAGAATG 1140 ATTAACCTAG ACACTGGGGT TAAGAGCAGA GAGAAAGGCC TGAAGCCAGA CACTTCCAGT 1200 GCCCCCCAAC CCCCCAAGGC AGGACAAACT TGGCCTCCCA GACCCACCAC TGGGTGGAAA 1260 GTGGATGCTG AGGAACCCCC TCCACCGCCC AACGCTGGGG CCTGGACACA GCTGGCAGGG 1320 TCACGGCCTC CAGCTGCAGT GTATCTGCTC CACTCTGGGG CCATTGCCCT CAAGCTCTGA 1380 GGTGCCAGAG CCATAGGGCG GGGTCCTGAG AAGGGGCAGT TCCAACCAGG CCAGGCCTGG 1440 TCAGCAGCTG TTTCTCTTCC CCACCCCCAC GGGCAGGCAG AAGCTGATGG GCTGCGGCTG 1500 CTGGAGCTGG GAAGGCCCAC CCTAGGGACA CCCAGGGGAC CTGCCCCTGC CTTCCCTCAA 1560 ACATAAAGAA AACAGTAAGC AAGTTGCCTA CCAGGGTGAG AAGAGATATG CCCAGCTGGA 1620 AGACAGGTGT GGGGGACCCC CAGAGCTGGG GACCCCAAAG GAAGGTGACA GCTGAACAAC 1680 CTGGGGGATG GACTGGCAGG GAGCAACCTA AACCCTAGCG CTACTGCAGC TGTGAGAACA 1740 ACCCTCACCC TCACCCTGGA GTTACAATAG GCGGGAAACG GGGAGGGGCC ACGCAAGGCA 1800 CTCGGCCCCA CCCAGACCCT GGGCTGGAAG 1830
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