Tag | Content |
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EnhancerAtlas ID | HS017-14906 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr18:3623790-3625180 |
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 | AAAAAAGGAA AACCCCCCTA GAAAATGCTT TTCCCGTTGC TTCCCTGCTA ATGGGCCTTT 60 TTCATCAGGG CAGCCTCCAG CCTTAGGATG TGGCCGGTCC CCGTGCGGAT GCCCGTTTCC 120 CCTCCTGCCT GCATTCATCT GACCGGTTCA GTGGGATCTG GTACTTTTCC TCCCTCCTCC 180 TCGTGCTGGG CTTCCACATC ATCCAGACAG CTGCTGCCAC ATTCCACCGC TCCAGCAGCG 240 GAAGTAAGGC ACATTTAGGC CCTTTCTGGG TGAGTGACAG CATTTGAGAT GAGATTAATC 300 AAATGCCAGT GTTAGGGGAA AGCAGCCTTT CCCTGAGTCA CCTCTGCTCC ACCTTTCTCA 360 TGACACAGAG CATGAGCCTG TCCAACGGTT GGCCTGTGCG TCAACCTCTG GCCAGGAGAC 420 AACGGGCGCC TGTGACCTGG GCGTGAACCG TCTGTTTGTG CGCATAGGTC TGACACTGCT 480 GCTGGGCGAG CCTGCGTGCC CCTGCCCCGC GGTCCATTGA CTGTGCCGCT GAGCACAGGC 540 AGGGATGTGT GCCTGTCGCC CTGGGCCGCT GTCCCCTGAC GGCAGATGAG ATATTCTTCC 600 AGCTCAACAC TGATGTTGCA GGGTTTTTCC TCACCTACCG CATGACGACT GAATGAAAGC 660 ATTCCAGGAA ACCAAAAGGG CTGGGCAGGC CTCTGGAATT TCAAAGCCGA CAGCCTGGCC 720 CTGCTGGCAG CTCATTTCTG CCGCGTCATT TTCTCTGAAC TGTAGGAGTA GTTTTGTAGC 780 AAACTTATCA CCAAAATCCC ACAAATGTTA AGCATTACCC TTCTTAGAAA GGAAAAGCCT 840 ACTTACTTTT CCCCATTGGA AGACTTCAAT TTTTTAAGAT TCAAGAAATC CCCAAAAGTC 900 ATGATAAAGA AGAGGGAAAA CAGACTGAGC ATACCCATCC CCTTTTAAAT TCAAATTTAT 960 TTTGTTTTTT TCTGCTTAGC TACAGGGAAG GTTTGATCAT ATCACATCTG AGTTAGGCCA 1020 TATGCACCCA GGGGGAATCT CAAGAGCAAA CTAATCTAAA CTCCAAGAAA TAGACCACTA 1080 AGACCCACCC AGGTAGTACT CACTGAACGC TCTTCCTGCC TCTCATAAGA ACCAAAAATA 1140 GCGGTTTCCC GCAGATGCTC CCAGAAGCAA AGTCTACCTA CCACACACAC AATATGCAGA 1200 AGGGAAAAAC CCAAGCCACA AGTCCCTAAA CGCCTGAGTC GTGACTCATG GAGGCTGTCC 1260 TCCACCCCTG CCAAGTATAA GAAATGATTT CTACCCACCC ACTTCTCTAA GGAGATGGTC 1320 CCTCATTCCT CTCTCCCGAG CAGGCTTCAC AGCCCCCTTC ATAGAGATGA AGCCCTAGTC 1380 ATTAAATGCC 1390
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