Tag | Content |
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EnhancerAtlas ID | HS044-06064 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr18:3623070-3626090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr18:3623995-3624006 | GACAGCTGCTG | + | 6.14 | Tcf12 | MA0521.1 | chr18:3623995-3624006 | GACAGCTGCTG | + | 6.02 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_02763 | chr18:3622267-3626272 | Astrocytes | SE_13339 | chr18:3621069-3626272 | CD34_Primary_RO01536 | SE_14380 | chr18:3620686-3627455 | CD4_Memory_Primary_7pool | SE_20735 | chr18:3621025-3626633 | CD8_Memory_7pool | SE_23414 | chr18:3623672-3625530 | Colon_Crypt_1 | SE_24111 | chr18:3623695-3624667 | Colon_Crypt_2 | SE_24111 | chr18:3624759-3625440 | Colon_Crypt_2 | SE_28047 | chr18:3623465-3625811 | Fetal_Intestine | SE_29024 | chr18:3623576-3625604 | Fetal_Intestine_Large | SE_29644 | chr18:3623207-3625384 | Fetal_Muscle | SE_31815 | chr18:3622925-3625600 | Gastric | SE_33785 | chr18:3622156-3626532 | HCC1954 | SE_34235 | chr18:3601188-3628195 | HCT-116 | SE_34627 | chr18:3620675-3627737 | HeLa | SE_36484 | chr18:3622231-3626476 | HMEC | SE_37649 | chr18:3621501-3626595 | HSMMtube | SE_39841 | chr18:3620699-3627829 | K562 | SE_44173 | chr18:3621676-3626130 | NHDF-Ad | SE_44760 | chr18:3621598-3626138 | NHLF | SE_46537 | chr18:3621539-3626487 | Osteoblasts | SE_47120 | chr18:3601015-3628781 | Panc1 | SE_50254 | chr18:3622960-3625633 | Sigmoid_Colon | SE_52285 | chr18:3621783-3625994 | Skeletal_Muscle_Myoblast | SE_52452 | chr18:3622290-3625714 | Small_Intestine | SE_56746 | chr18:3623021-3626737 | VACO_400 | SE_57446 | chr18:3623391-3624648 | VACO_503 | SE_57446 | chr18:3624737-3625557 | VACO_503 | SE_64064 | chr18:3621712-3626001 | HSMM | SE_64950 | chr18:3622265-3626251 | NHEK | SE_67704 | chr18:3621437-3626982 | u87 | SE_68903 | chr18:3623657-3625587 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr18 | 3624841 | 3625119 | chr18 | 3623872 | 3624258 | chr18 | 3624338 | 3624601 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I003615 | chr18 | 3615106 | 3627844 |
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Enhancer Sequence | TGGGATTACA CGCGTGAGCC ACCAGCCTGG CCTGATTTCA GTACTGGAAT GGCCTCATGT 60 CAGCTGGGTG ATCTTGTGTG CTGCCTCTCT GTGTCCCCAT GTCCTCACTG GTGAAACAGG 120 CATGCTAAAA GCATTGATTT AAGAGAGTTG TTGAGAGGAT CACATGAGAT AATCAAGGAA 180 AAAGTCTTAG ATCAGGGCCT GGAACAAAGT AAATGTTTAA TCCTATTAAT GCAATTAATT 240 GTGGTTAATG ACATGTCATA ATTAATAGCT ATGATTATTT TCACGAGCCC TGACATTATC 300 TTCCATTTCC AGGCTTCGCA TGTATAAGAG GTCCTAGACA CAAATTCACC TACACAAGGG 360 ATTCAGTCCG TCTTAGGTTC TGCTAATGAC AACTCTTCTT GAAGTTCTTC AAGGCCGTGT 420 GAAAAGGAAA AGCCAGCCGG GCACAGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGG 480 CTGAGGCGGG CGGATCACCT GAGGTCAGGA GTGCGAGACC AGCCTGGCCA ATGTGTCTCT 540 ACTAAAAATA CAAAAATCAG CCGGGCGTGG TGGCGCATGC CTGTAATCCC AGCTACTCAG 600 GAGCCTGAGG CAGGAGAATC GCTTGAACCT GGGAGGCGGA GCTTGCAGTG AGCCGAGGTC 660 ACACTACTGC ACCCCAGCCT GAGAGACAGA GCAAGACTCC GTCTCAAAAA AAAAAAAAAA 720 AAAAAAGGAA AACCCCCCTA GAAAATGCTT TTCCCGTTGC TTCCCTGCTA ATGGGCCTTT 780 TTCATCAGGG CAGCCTCCAG CCTTAGGATG TGGCCGGTCC CCGTGCGGAT GCCCGTTTCC 840 CCTCCTGCCT GCATTCATCT GACCGGTTCA GTGGGATCTG GTACTTTTCC TCCCTCCTCC 900 TCGTGCTGGG CTTCCACATC ATCCAGACAG CTGCTGCCAC ATTCCACCGC TCCAGCAGCG 960 GAAGTAAGGC ACATTTAGGC CCTTTCTGGG TGAGTGACAG CATTTGAGAT GAGATTAATC 1020 AAATGCCAGT GTTAGGGGAA AGCAGCCTTT CCCTGAGTCA CCTCTGCTCC ACCTTTCTCA 1080 TGACACAGAG CATGAGCCTG TCCAACGGTT GGCCTGTGCG TCAACCTCTG GCCAGGAGAC 1140 AACGGGCGCC TGTGACCTGG GCGTGAACCG TCTGTTTGTG CGCATAGGTC TGACACTGCT 1200 GCTGGGCGAG CCTGCGTGCC CCTGCCCCGC GGTCCATTGA CTGTGCCGCT GAGCACAGGC 1260 AGGGATGTGT GCCTGTCGCC CTGGGCCGCT GTCCCCTGAC GGCAGATGAG ATATTCTTCC 1320 AGCTCAACAC TGATGTTGCA GGGTTTTTCC TCACCTACCG CATGACGACT GAATGAAAGC 1380 ATTCCAGGAA ACCAAAAGGG CTGGGCAGGC CTCTGGAATT TCAAAGCCGA CAGCCTGGCC 1440 CTGCTGGCAG CTCATTTCTG CCGCGTCATT TTCTCTGAAC TGTAGGAGTA GTTTTGTAGC 1500 AAACTTATCA CCAAAATCCC ACAAATGTTA AGCATTACCC TTCTTAGAAA GGAAAAGCCT 1560 ACTTACTTTT CCCCATTGGA AGACTTCAAT TTTTTAAGAT TCAAGAAATC CCCAAAAGTC 1620 ATGATAAAGA AGAGGGAAAA CAGACTGAGC ATACCCATCC CCTTTTAAAT TCAAATTTAT 1680 TTTGTTTTTT TCTGCTTAGC TACAGGGAAG GTTTGATCAT ATCACATCTG AGTTAGGCCA 1740 TATGCACCCA GGGGGAATCT CAAGAGCAAA CTAATCTAAA CTCCAAGAAA TAGACCACTA 1800 AGACCCACCC AGGTAGTACT CACTGAACGC TCTTCCTGCC TCTCATAAGA ACCAAAAATA 1860 GCGGTTTCCC GCAGATGCTC CCAGAAGCAA AGTCTACCTA CCACACACAC AATATGCAGA 1920 AGGGAAAAAC CCAAGCCACA AGTCCCTAAA CGCCTGAGTC GTGACTCATG GAGGCTGTCC 1980 TCCACCCCTG CCAAGTATAA GAAATGATTT CTACCCACCC ACTTCTCTAA GGAGATGGTC 2040 CCTCATTCCT CTCTCCCGAG CAGGCTTCAC AGCCCCCTTC ATAGAGATGA AGCCCTAGTC 2100 ATTAAATGCC CAGTGATGTT ACGACTGCCA AATTCTATGA CTATTTGGAA AGTTTTATCA 2160 GGTATGGATA CACTCCACCT ATTTGCTTAG GTGGCCAAGA TCTCTGTGCA GTTGCACAGA 2220 CAGTTTCTGT CCTCCCACCC CGTGAGAGGT TGTGTGTGTG TTTGCGGGGG CTGGGAAGCT 2280 AATGGAGGGA AGGAGAGACC TCCTCAGGTG AGTCACCTTG CAGTGGAACT GCTTCCTGTG 2340 TGTGTGAAGT TCTTCAAGGA GGCACCACTT CACGCAATGC CCCAAACAGA AAAATCGAAG 2400 CAAATTAGCA AATTATTTTC TAGGAGATTA GATGTTGGAC AACTTCAAGC TTTCACAATA 2460 GAAAATGGCT TGTTTTAAGG CAGTTAAACC CAAAGCATGC CTTTTTTGGG GTTTTGTTTA 2520 TGAATATGTT GTAATCTAAG AAGAGTAATG TTCTTACAGA AAAATTAGAC CTTCATGATT 2580 GCAATCTAAG TGAGAGGCAA TTAGGCTTAT TTTTCTTAGA GATTAGTACA TCATGTTAGT 2640 TCAGAAAGCA TTTGTAAAAC AGAAAAAAAA AGGAAATCAT AAATATCAAT TTCATCTTAA 2700 CACAATGCAA CTATCACTGT TCTCAACCTG AGTTCTTAAT TTCTGGCATG TCACAAATTC 2760 CTTGAACTAC CAATGTTGAA CTAACCTCCC CTGACCCAGG GAGTTGAATA GTTTTTTCAA 2820 AGGATATGAT CAAATCTCTG TTCATGCATG CCTACATTTA TTCATTTTCC AAAAGCATAA 2880 ATTAATTCTG AGGGACAGAA AGTAGACTTG TGCTTGCCTA GGTTTGTGGG AGATGAAAAT 2940 GTGGCTGGGA GCCATGGCTC ACACCTGTAA TCCCAGCATT TTAGGAGGCT GAGGCAGGAG 3000 GATCATTTCA GCCCAGGAAT 3020
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