Tag | Content |
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EnhancerAtlas ID | HS048-02539 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:159891230-159893220 |
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 | GCCTCCAGAA GCCAGAAAAG GGAAGGAAAT AGATTCACCC AAAAACCCCA GAAGGAACAC 60 AGCTCTGCCA ACACCTGTAT TTTAGCCAGT GAGACCCCTG TTGAGTCTGT AGAACTGTAA 120 GATGCTGTAT TTGTGTTGCT TTAAATCACT AAGCTTGTAG CAATTTGTTA CAGCAGAAAT 180 AGGAAACTAA TACAGGAGCC CTGGGTGATA TTTTTGGGGA AACCTGGAGA AGAGAAGGCA 240 AGACGGGGAA ATACACAGGA GGGTTTCTTT AACTTCGTTG GAGGAGCTTG ATTAGCAAGA 300 ACTGGGTGGT TTCCCGACCA ATGGCCTGAG TTGGCGGACC TCACTGTGGC AGTGTGTTCC 360 CACCACACTC ACCACCTGGG TCTGACACTC AGGGGCTGAG CAAGACCCGG GCATGGTATG 420 GATGCCAAGG GGAGCCAAGA ACCAAGAATG GGCCACAGTC CCCATTTTCT GTCCCATCCC 480 CACCCTGGTT TGGCTTTTCT CTCTTCTCCA AAACAGAGCT AGCTGTCAGG CTGCTCACGA 540 AAGGGGACCC CCAGGACAGG CATCTGCGTT CAAGGGGAAG AAAGAGAGCC ACCCCTTCTA 600 ACCACATCTG GCTCCAGGCC AGGTTGGCCT TCAGGGATGA AGTCACTCCA GCTCCCCCTC 660 TCCCACACAC CCAGGTTAAA CAATCCCGTC ACCCCCTCTC AATGGACCTT GGGGCTCTGC 720 GAAATACAAG GGGACCAGCC TGCCTCAAAC CCTCAACACC TCTCGGCCGC AGAGGCTGTG 780 TCTTGGGCCA GTCCCTCCCG TCCCGACTCC AACATGGCTG CTCCTTTTTA CCCCAGCTTA 840 TCAAGCTGCA CATTTCCGGC AGATCCTCCC CTAAATCAGT TATTTTTAAA CCTCATTAAG 900 AGCAACCCGC CCCCTCCACT TCCCCCAGCC CGAAAGCTGG GCCAGATAAA TGTCAGTCTG 960 GGCCCCGACC CACAGCGCCA GGCACACACA CCATCAGCTT GGGGAAGGCA GGCGGGGTGG 1020 GGTGGCTGAG TTCTGAGGAG AAACCAAGAG AAGCATCCCT GCCCTTCCCA GAGGCCACTC 1080 CACCATAGAA ACCTCTAACC TCTGATGCAC AGGGGAATGG CTGGAAGACA GGTAGGAAGA 1140 GGAAGGGGCT AAGAGCTACT ACCACCAGTA AGCCCCCTTT CCGCAGCCCA GTTCCAGACC 1200 TCTCTCCTGG GAGTGGCTGT GCTCAGGGCT GTTTCCAGGG ACCAAGTGGC CTGAGGCTCG 1260 GGGATCACCA TGGCACAGGT AAAGAAAGGG CAGGAGAATG ATTAACCTAG ACACTGGGGT 1320 TAAGAGCAGA GAGAAAGGCC TGAAGCCAGA CACTTCCAGT GCCCCCCAAC CCCCCAAGGC 1380 AGGACAAACT TGGCCTCCCA GACCCACCAC TGGGTGGAAA GTGGATGCTG AGGAACCCCC 1440 TCCACCGCCC AACGCTGGGG CCTGGACACA GCTGGCAGGG TCACGGCCTC CAGCTGCAGT 1500 GTATCTGCTC CACTCTGGGG CCATTGCCCT CAAGCTCTGA GGTGCCAGAG CCATAGGGCG 1560 GGGTCCTGAG AAGGGGCAGT TCCAACCAGG CCAGGCCTGG TCAGCAGCTG TTTCTCTTCC 1620 CCACCCCCAC GGGCAGGCAG AAGCTGATGG GCTGCGGCTG CTGGAGCTGG GAAGGCCCAC 1680 CCTAGGGACA CCCAGGGGAC CTGCCCCTGC CTTCCCTCAA ACATAAAGAA AACAGTAAGC 1740 AAGTTGCCTA CCAGGGTGAG AAGAGATATG CCCAGCTGGA AGACAGGTGT GGGGGACCCC 1800 CAGAGCTGGG GACCCCAAAG GAAGGTGACA GCTGAACAAC CTGGGGGATG GACTGGCAGG 1860 GAGCAACCTA AACCCTAGCG CTACTGCAGC TGTGAGAACA ACCCTCACCC TCACCCTGGA 1920 GTTACAATAG GCGGGAAACG GGGAGGGGCC ACGCAAGGCA CTCGGCCCCA CCCAGACCCT 1980 GGGCTGGAAG 1990
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