Tag | Content |
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EnhancerAtlas ID | HS045-29339 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr18:3623570-3625780 |
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 | GAGGTCAGGA GTGCGAGACC AGCCTGGCCA ATGTGTCTCT ACTAAAAATA CAAAAATCAG 60 CCGGGCGTGG TGGCGCATGC CTGTAATCCC AGCTACTCAG GAGCCTGAGG CAGGAGAATC 120 GCTTGAACCT GGGAGGCGGA GCTTGCAGTG AGCCGAGGTC ACACTACTGC ACCCCAGCCT 180 GAGAGACAGA GCAAGACTCC GTCTCAAAAA AAAAAAAAAA AAAAAAGGAA AACCCCCCTA 240 GAAAATGCTT TTCCCGTTGC TTCCCTGCTA ATGGGCCTTT TTCATCAGGG CAGCCTCCAG 300 CCTTAGGATG TGGCCGGTCC CCGTGCGGAT GCCCGTTTCC CCTCCTGCCT GCATTCATCT 360 GACCGGTTCA GTGGGATCTG GTACTTTTCC TCCCTCCTCC TCGTGCTGGG CTTCCACATC 420 ATCCAGACAG CTGCTGCCAC ATTCCACCGC TCCAGCAGCG GAAGTAAGGC ACATTTAGGC 480 CCTTTCTGGG TGAGTGACAG CATTTGAGAT GAGATTAATC AAATGCCAGT GTTAGGGGAA 540 AGCAGCCTTT CCCTGAGTCA CCTCTGCTCC ACCTTTCTCA TGACACAGAG CATGAGCCTG 600 TCCAACGGTT GGCCTGTGCG TCAACCTCTG GCCAGGAGAC AACGGGCGCC TGTGACCTGG 660 GCGTGAACCG TCTGTTTGTG CGCATAGGTC TGACACTGCT GCTGGGCGAG CCTGCGTGCC 720 CCTGCCCCGC GGTCCATTGA CTGTGCCGCT GAGCACAGGC AGGGATGTGT GCCTGTCGCC 780 CTGGGCCGCT GTCCCCTGAC GGCAGATGAG ATATTCTTCC AGCTCAACAC TGATGTTGCA 840 GGGTTTTTCC TCACCTACCG CATGACGACT GAATGAAAGC ATTCCAGGAA ACCAAAAGGG 900 CTGGGCAGGC CTCTGGAATT TCAAAGCCGA CAGCCTGGCC CTGCTGGCAG CTCATTTCTG 960 CCGCGTCATT TTCTCTGAAC TGTAGGAGTA GTTTTGTAGC AAACTTATCA CCAAAATCCC 1020 ACAAATGTTA AGCATTACCC TTCTTAGAAA GGAAAAGCCT ACTTACTTTT CCCCATTGGA 1080 AGACTTCAAT TTTTTAAGAT TCAAGAAATC CCCAAAAGTC ATGATAAAGA AGAGGGAAAA 1140 CAGACTGAGC ATACCCATCC CCTTTTAAAT TCAAATTTAT TTTGTTTTTT TCTGCTTAGC 1200 TACAGGGAAG GTTTGATCAT ATCACATCTG AGTTAGGCCA TATGCACCCA GGGGGAATCT 1260 CAAGAGCAAA CTAATCTAAA CTCCAAGAAA TAGACCACTA AGACCCACCC AGGTAGTACT 1320 CACTGAACGC TCTTCCTGCC TCTCATAAGA ACCAAAAATA GCGGTTTCCC GCAGATGCTC 1380 CCAGAAGCAA AGTCTACCTA CCACACACAC AATATGCAGA AGGGAAAAAC CCAAGCCACA 1440 AGTCCCTAAA CGCCTGAGTC GTGACTCATG GAGGCTGTCC TCCACCCCTG CCAAGTATAA 1500 GAAATGATTT CTACCCACCC ACTTCTCTAA GGAGATGGTC CCTCATTCCT CTCTCCCGAG 1560 CAGGCTTCAC AGCCCCCTTC ATAGAGATGA AGCCCTAGTC ATTAAATGCC CAGTGATGTT 1620 ACGACTGCCA AATTCTATGA CTATTTGGAA AGTTTTATCA GGTATGGATA CACTCCACCT 1680 ATTTGCTTAG GTGGCCAAGA TCTCTGTGCA GTTGCACAGA CAGTTTCTGT CCTCCCACCC 1740 CGTGAGAGGT TGTGTGTGTG TTTGCGGGGG CTGGGAAGCT AATGGAGGGA AGGAGAGACC 1800 TCCTCAGGTG AGTCACCTTG CAGTGGAACT GCTTCCTGTG TGTGTGAAGT TCTTCAAGGA 1860 GGCACCACTT CACGCAATGC CCCAAACAGA AAAATCGAAG CAAATTAGCA AATTATTTTC 1920 TAGGAGATTA GATGTTGGAC AACTTCAAGC TTTCACAATA GAAAATGGCT TGTTTTAAGG 1980 CAGTTAAACC CAAAGCATGC CTTTTTTGGG GTTTTGTTTA TGAATATGTT GTAATCTAAG 2040 AAGAGTAATG TTCTTACAGA AAAATTAGAC CTTCATGATT GCAATCTAAG TGAGAGGCAA 2100 TTAGGCTTAT TTTTCTTAGA GATTAGTACA TCATGTTAGT TCAGAAAGCA TTTGTAAAAC 2160 AGAAAAAAAA AGGAAATCAT AAATATCAAT TTCATCTTAA CACAATGCAA 2210
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