| Tag | Content |
|---|
EnhancerAtlas ID | HS118-09076 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr19:6055860-6058630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:6057682-6057701 | TGGCCTCCAGATGGTACCA | + | 6.14 | | ESRRB | MA0141.3 | chr19:6057132-6057143 | TTTGACCTTGA | - | 6.14 | | Esrra | MA0592.2 | chr19:6057133-6057144 | TTGACCTTGAA | - | 6.14 | | MYC | MA0147.3 | chr19:6057633-6057645 | AGGCACGTGGCC | - | 6.07 | | NFYA | MA0060.3 | chr19:6057602-6057613 | TCTGATTGGCT | - | 6.32 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_00353 | chr19:6054967-6063609 | Adipose_Nuclei | | SE_00846 | chr19:6056545-6057132 | Adipose_Tissue | | SE_00846 | chr19:6057712-6058063 | Adipose_Tissue | | SE_01604 | chr19:6055906-6064951 | Aorta | | SE_09597 | chr19:6055833-6059394 | CD14 | | SE_12907 | chr19:6056251-6058341 | CD34_Primary_RO01480 | | SE_13400 | chr19:6055987-6059381 | CD34_Primary_RO01536 | | SE_14082 | chr19:6056159-6059147 | CD34_Primary_RO01549 | | SE_23458 | chr19:6055868-6059019 | Colon_Crypt_1 | | SE_24248 | chr19:6056123-6058298 | Colon_Crypt_2 | | SE_25797 | chr19:6054521-6073197 | Duodenum_Smooth_Muscle | | SE_26679 | chr19:6055890-6065109 | Esophagus | | SE_29788 | chr19:6056121-6059312 | Fetal_Muscle | | SE_35921 | chr19:6055716-6059103 | HMEC | | SE_37314 | chr19:6055988-6058832 | HSMMtube | | SE_38048 | chr19:6055954-6068597 | HUVEC | | SE_42288 | chr19:6055959-6059242 | Lung | | SE_44165 | chr19:6055660-6059268 | NHDF-Ad | | SE_44879 | chr19:6056229-6058691 | NHLF | | SE_49210 | chr19:6055928-6064945 | Right_Atrium | | SE_52794 | chr19:6055944-6059172 | Small_Intestine | | SE_54507 | chr19:6054642-6073245 | Stomach_Smooth_Muscle | | SE_64265 | chr19:6055971-6059135 | NHEK | | SE_65533 | chr19:6055391-6059553 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I006055 | chr19 | 6055612 | 6069370 |
|
Enhancer Sequence | GGAATACTAC TGGAATACTC TTCATGAATA GAAAGGAATT AATTACTGAA ATTCACAATG 60
CATGGATGAA TCTCAAAATC ATTACGCTGA GTGAAAGAAG TTGAGTCCAA AAGAGTAGAT 120
GAGTAGAGTG GATTAAAACT AAAGTTAAAA AAAAATCATA ATAGTGGGTG GGGGGGCAGG 180
TGGCGGTGGG CGAGAGTGAC TGGAAAGGGA CAGGAGGGGA CACTCCAGTG AGATGGACGC 240
ATTCTGTATG ATAATACAGT GTGCGGTTAC ATGGAGTCGT GATTTGTCAA AATTAGCCAG 300
CTAAGGTTTG TGCACTTACT GTATGTGAAT TTTAACAATG ACAACGAAGC CTGTAAAAAT 360
ACAAGGGTGG AGAGGAGGAC GGAGAGTGGG TACAGGTATC CAGGTGTTAT AAGAATGGCA 420
GGACCCTGAC ACCCTGTAGA GGGTGGTGGC TTCATAAGTT TCATTGCATT GTGTATTTAC 480
TTTGTGGATG TTTGAAATTT CCATGATAAG GAGTTAAACA AACACACACA CAAGACACCA 540
GCGATGAGCA GGAGTGGCTC ATGATCCTGG CGGTGCTTCC AGGTAAGCGC AGTAGCTCAC 600
ATGGTCCTCC CAGAAGGGGT GATGCTGGAT CCTGAGTAAC TCCTCCACCT GGCAGAGGAG 660
AGCGCAGCAG AGAGTGGGCA GAGGGCAGGG CCCCGAGGGC GTGGGTGTAC TCAAGGTAAA 720
GTCCACAGGG CACAGGGACG CACACTGTGG AGCACCTTTG CAGCACCCAG TTTGGGAACC 780
CCTCAATCCA GTGCAAGACA GTAGATGTGA GTGAGTGGAG GCCATGCTTC TTCTCTGAAC 840
CTGAATCTGC TGTGGGAACT TGGACCCATT CAGTGACTGC CCTGCCGTCC TTGCTTTCTC 900
GCGTTCCTTT GTCCTCTCTT CTGTTTTTCT TCCTGTGGCG AGGACCTGGG CAGTCTTACT 960
TTGACTGCCT TCCCCTGTGT CCTCTTAGAC TGGGTTACAG GAGCCTCGGA ACAGCCAATA 1020
TAAAGGGGAG GGGCCGCAAC ACGACCTGTC ACCCAGCCTG GCCCTGCCTG GCCAACGGGC 1080
TTGGCTGGCC CAAAGCTCCC TCCCTCGTGC CTCAGAAATA TGCCCGGAGT GCTGTTTATA 1140
AGCTGAGCAC GTTTCATTTA CCATCTGGTC CAAGATCAGG GCGGGCATGA AATAAAGGGG 1200
AAAAGCACAG AACCAGCGGC GCAATTTCCC CTCCTTGGCC GGCACCAGCC TTTGGAATCC 1260
ACGAAACGCT CATTTGACCT TGAACGAACA TTCAAGTGAA CCAGATGCGC ACTTGACCTT 1320
TTGGAGCCAC TGCTGAGTCA AACGCGCCAG TGGGAACATC TCCCGTGGCT TCCTGACTTC 1380
ATGTGAGGGG GCACAGGAGA GACGCAGCTA GAAGCAGCCC TGGACTACGG CCGTGATGAA 1440
TGAATCTGCC TGGGCACAAA GGGAAGAGGC TTCTGTTTAC AGAAAAATAC TCCCATCACC 1500
TAGTAACCAG CAATGTCAGG AAAGGAAATG CAGAAAACGC TGAGAGCAAT TTCTGGGCCC 1560
GTTCCTGGCT GAGCCGCTGA CTCACTGCGA CCTTAAGCAA TCTCTCTTCT ATTCCTGTTC 1620
CTCCATATGC CAAATGGAGC TGTCACCTGC CTCACATAGT TCAGATCAGT ATTTAGACAA 1680
TGTTTTGTCA TCTTTGGTGA TAATTGGGGC AGAGTTAGCT GAGTGGTTTT AGTTACCTTC 1740
ATTCTGATTG GCTGATGAGC CTCGGTGTTT GGGAGGCACG TGGCCTCCTC CGGCCATCAG 1800
CTCCTCCTCT CCTGGTACTC GCTGGCCTCC AGATGGTACC AGAGTTCATC TGCCCTAAGA 1860
AAGCAATTAA TTTCCTCCCT CTGAACAAGA AGGAACAAGC CCGGAGTGCT CTCAGGAGTA 1920
CCAGTTGCTT CAAAGCCCAG ATTCTGTCCT GGTAGCTTGT CTTAACACTC CCAGTGTCAT 1980
TAGGCTGCCC AGAAAAGTCT TGTCCGTTTC CTTCTCCCGG CTCCCCTCTG AGGGCCAGGT 2040
CCTCGGAGTA AGTGATGCGT GTTTTAAGAT TCTGTCCTCA CTGTTCAGGC TTGTGTGGCC 2100
TGGCCCCACG CACAGGGAGG ACACCTCCAA GCCATCTCCT TGCCGAAAAG TGGATTCTCG 2160
AACCCTCCTT GATGGTGGAA CCATGTCCTT TCTGGCACCA GGATTACTCC CTGTGGACCC 2220
AGTTGGTTCT CAGTGCCAAG AGTTATTACT CTGCCCTGAT AATCACCAAA GATGACAGTG 2280
TGTGTCCCCA CTTGGCACTG TGGACATTGG GGACGGATCC ATCTCTGGGC TGGGGCCGTC 2340
CTGAGCACTG CAGGGTGCTG AGCAGCATCC CTGGCCTCCG CTCACTCCAT GCCAAGAGCA 2400
CCCCCAGTTG TGACAACCAC AGATGTTCCC AGACATTGCC CAGTGTCCCC TGGGGCGCAG 2460
AAGGACCTCT GTTCAAAATG GATTTGTGAT GTCTAAGAAG GGGTCTGGAC AAACAGCCCC 2520
CGAGTAAAAC AGGCCTGTAG ACAGGGTGAG AACAGGAAGA TGAAAAAGGA GAGTAGGCAG 2580
GATGCAAAAT CATGACAATT CAGCCAGGCA AGGAGTGTGA AATAAATGAA CAGGACCCTC 2640
TGAAGGCTAC CCACACATTC CAGAGCAGCA GGCTTCAATG CACACCAAGG GCAACCATCG 2700
TTCCCTCCGT GCCTAAGCCA CGGGGGTGCC CGTCATTCCT CACTTTTGGG TTTTTTTTTT 2760
TTCTCCTCTT 2770
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