Tag | Content |
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EnhancerAtlas ID | HS051-12797 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr18:3623840-3625630 |
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 | ATGGGCCTTT TTCATCAGGG CAGCCTCCAG CCTTAGGATG TGGCCGGTCC CCGTGCGGAT 60 GCCCGTTTCC CCTCCTGCCT GCATTCATCT GACCGGTTCA GTGGGATCTG GTACTTTTCC 120 TCCCTCCTCC TCGTGCTGGG CTTCCACATC ATCCAGACAG CTGCTGCCAC ATTCCACCGC 180 TCCAGCAGCG GAAGTAAGGC ACATTTAGGC CCTTTCTGGG TGAGTGACAG CATTTGAGAT 240 GAGATTAATC AAATGCCAGT GTTAGGGGAA AGCAGCCTTT CCCTGAGTCA CCTCTGCTCC 300 ACCTTTCTCA TGACACAGAG CATGAGCCTG TCCAACGGTT GGCCTGTGCG TCAACCTCTG 360 GCCAGGAGAC AACGGGCGCC TGTGACCTGG GCGTGAACCG TCTGTTTGTG CGCATAGGTC 420 TGACACTGCT GCTGGGCGAG CCTGCGTGCC CCTGCCCCGC GGTCCATTGA CTGTGCCGCT 480 GAGCACAGGC AGGGATGTGT GCCTGTCGCC CTGGGCCGCT GTCCCCTGAC GGCAGATGAG 540 ATATTCTTCC AGCTCAACAC TGATGTTGCA GGGTTTTTCC TCACCTACCG CATGACGACT 600 GAATGAAAGC ATTCCAGGAA ACCAAAAGGG CTGGGCAGGC CTCTGGAATT TCAAAGCCGA 660 CAGCCTGGCC CTGCTGGCAG CTCATTTCTG CCGCGTCATT TTCTCTGAAC TGTAGGAGTA 720 GTTTTGTAGC AAACTTATCA CCAAAATCCC ACAAATGTTA AGCATTACCC TTCTTAGAAA 780 GGAAAAGCCT ACTTACTTTT CCCCATTGGA AGACTTCAAT TTTTTAAGAT TCAAGAAATC 840 CCCAAAAGTC ATGATAAAGA AGAGGGAAAA CAGACTGAGC ATACCCATCC CCTTTTAAAT 900 TCAAATTTAT TTTGTTTTTT TCTGCTTAGC TACAGGGAAG GTTTGATCAT ATCACATCTG 960 AGTTAGGCCA TATGCACCCA GGGGGAATCT CAAGAGCAAA CTAATCTAAA CTCCAAGAAA 1020 TAGACCACTA AGACCCACCC AGGTAGTACT CACTGAACGC TCTTCCTGCC TCTCATAAGA 1080 ACCAAAAATA GCGGTTTCCC GCAGATGCTC CCAGAAGCAA AGTCTACCTA CCACACACAC 1140 AATATGCAGA AGGGAAAAAC CCAAGCCACA AGTCCCTAAA CGCCTGAGTC GTGACTCATG 1200 GAGGCTGTCC TCCACCCCTG CCAAGTATAA GAAATGATTT CTACCCACCC ACTTCTCTAA 1260 GGAGATGGTC CCTCATTCCT CTCTCCCGAG CAGGCTTCAC AGCCCCCTTC ATAGAGATGA 1320 AGCCCTAGTC ATTAAATGCC CAGTGATGTT ACGACTGCCA AATTCTATGA CTATTTGGAA 1380 AGTTTTATCA GGTATGGATA CACTCCACCT ATTTGCTTAG GTGGCCAAGA TCTCTGTGCA 1440 GTTGCACAGA CAGTTTCTGT CCTCCCACCC CGTGAGAGGT TGTGTGTGTG TTTGCGGGGG 1500 CTGGGAAGCT AATGGAGGGA AGGAGAGACC TCCTCAGGTG AGTCACCTTG CAGTGGAACT 1560 GCTTCCTGTG TGTGTGAAGT TCTTCAAGGA GGCACCACTT CACGCAATGC CCCAAACAGA 1620 AAAATCGAAG CAAATTAGCA AATTATTTTC TAGGAGATTA GATGTTGGAC AACTTCAAGC 1680 TTTCACAATA GAAAATGGCT TGTTTTAAGG CAGTTAAACC CAAAGCATGC CTTTTTTGGG 1740 GTTTTGTTTA TGAATATGTT GTAATCTAAG AAGAGTAATG TTCTTACAGA 1790
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