Tag | Content |
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EnhancerAtlas ID | HS194-02472 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr18:3623730-3625600 |
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 | ACACTACTGC ACCCCAGCCT GAGAGACAGA GCAAGACTCC GTCTCAAAAA AAAAAAAAAA 60 AAAAAAGGAA AACCCCCCTA GAAAATGCTT TTCCCGTTGC TTCCCTGCTA ATGGGCCTTT 120 TTCATCAGGG CAGCCTCCAG CCTTAGGATG TGGCCGGTCC CCGTGCGGAT GCCCGTTTCC 180 CCTCCTGCCT GCATTCATCT GACCGGTTCA GTGGGATCTG GTACTTTTCC TCCCTCCTCC 240 TCGTGCTGGG CTTCCACATC ATCCAGACAG CTGCTGCCAC ATTCCACCGC TCCAGCAGCG 300 GAAGTAAGGC ACATTTAGGC CCTTTCTGGG TGAGTGACAG CATTTGAGAT GAGATTAATC 360 AAATGCCAGT GTTAGGGGAA AGCAGCCTTT CCCTGAGTCA CCTCTGCTCC ACCTTTCTCA 420 TGACACAGAG CATGAGCCTG TCCAACGGTT GGCCTGTGCG TCAACCTCTG GCCAGGAGAC 480 AACGGGCGCC TGTGACCTGG GCGTGAACCG TCTGTTTGTG CGCATAGGTC TGACACTGCT 540 GCTGGGCGAG CCTGCGTGCC CCTGCCCCGC GGTCCATTGA CTGTGCCGCT GAGCACAGGC 600 AGGGATGTGT GCCTGTCGCC CTGGGCCGCT GTCCCCTGAC GGCAGATGAG ATATTCTTCC 660 AGCTCAACAC TGATGTTGCA GGGTTTTTCC TCACCTACCG CATGACGACT GAATGAAAGC 720 ATTCCAGGAA ACCAAAAGGG CTGGGCAGGC CTCTGGAATT TCAAAGCCGA CAGCCTGGCC 780 CTGCTGGCAG CTCATTTCTG CCGCGTCATT TTCTCTGAAC TGTAGGAGTA GTTTTGTAGC 840 AAACTTATCA CCAAAATCCC ACAAATGTTA AGCATTACCC TTCTTAGAAA GGAAAAGCCT 900 ACTTACTTTT CCCCATTGGA AGACTTCAAT TTTTTAAGAT TCAAGAAATC CCCAAAAGTC 960 ATGATAAAGA AGAGGGAAAA CAGACTGAGC ATACCCATCC CCTTTTAAAT TCAAATTTAT 1020 TTTGTTTTTT TCTGCTTAGC TACAGGGAAG GTTTGATCAT ATCACATCTG AGTTAGGCCA 1080 TATGCACCCA GGGGGAATCT CAAGAGCAAA CTAATCTAAA CTCCAAGAAA TAGACCACTA 1140 AGACCCACCC AGGTAGTACT CACTGAACGC TCTTCCTGCC TCTCATAAGA ACCAAAAATA 1200 GCGGTTTCCC GCAGATGCTC CCAGAAGCAA AGTCTACCTA CCACACACAC AATATGCAGA 1260 AGGGAAAAAC CCAAGCCACA AGTCCCTAAA CGCCTGAGTC GTGACTCATG GAGGCTGTCC 1320 TCCACCCCTG CCAAGTATAA GAAATGATTT CTACCCACCC ACTTCTCTAA GGAGATGGTC 1380 CCTCATTCCT CTCTCCCGAG CAGGCTTCAC AGCCCCCTTC ATAGAGATGA AGCCCTAGTC 1440 ATTAAATGCC CAGTGATGTT ACGACTGCCA AATTCTATGA CTATTTGGAA AGTTTTATCA 1500 GGTATGGATA CACTCCACCT ATTTGCTTAG GTGGCCAAGA TCTCTGTGCA GTTGCACAGA 1560 CAGTTTCTGT CCTCCCACCC CGTGAGAGGT TGTGTGTGTG TTTGCGGGGG CTGGGAAGCT 1620 AATGGAGGGA AGGAGAGACC TCCTCAGGTG AGTCACCTTG CAGTGGAACT GCTTCCTGTG 1680 TGTGTGAAGT TCTTCAAGGA GGCACCACTT CACGCAATGC CCCAAACAGA AAAATCGAAG 1740 CAAATTAGCA AATTATTTTC TAGGAGATTA GATGTTGGAC AACTTCAAGC TTTCACAATA 1800 GAAAATGGCT TGTTTTAAGG CAGTTAAACC CAAAGCATGC CTTTTTTGGG GTTTTGTTTA 1860 TGAATATGTT 1870
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