| Tag | Content |
|---|
EnhancerAtlas ID | HS095-14599 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr19:11001550-11003510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF740 | MA0753.2 | chr19:11002287-11002300 | GTTGGGGGGGTGG | - | 6.07 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23673 | chr19:11001496-11003518 | Colon_Crypt_1 | | SE_24532 | chr19:11001499-11002816 | Colon_Crypt_2 | | SE_24532 | chr19:11002850-11003408 | Colon_Crypt_2 | | SE_30825 | chr19:11001493-11003878 | Fetal_Muscle | | SE_48197 | chr19:11001474-11008637 | Psoas_Muscle | | SE_51520 | chr19:11001498-11008729 | Skeletal_Muscle | | SE_68858 | chr19:11001508-11002892 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 11002861 | 11003310 | | chr19 | 11002008 | 11002828 | | chr19 | 11003000 | 11003314 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I010890 | chr19 | 11001540 | 11003913 |
|
Enhancer Sequence | GAGGATTGCT TCTTGAGCAC AGGAGGTCGA GGCTGCAGTG TGCTATGACT GGGCGGGCCA 60
TTGCACTCCA GCCTGGGTGA CAGAGGGAGA CCAAAACTGA GTCAGTGTTC CCAAGCAGTG 120
TGTGAAGCTG ATTCTCTGTC AGCCACGTGC CAGATGGGTT GGGTCCCAGG GGTGGCCACC 180
TGGGGGACAG GGCCAGACAC TTGTTCTGGG CCCAATATGG CCTTGTGTCC AGAACTCTCT 240
CGGTGGCTCC TTCTCTCGAC CCTTTGCCTT GAGCCGGAGC ACTGTGGGGA CACAGGAACC 300
AAGACTGGTG TTTTGTGCCA ATGCCACACT ACTGTGTGCC CGTGGGTCTT GGGCCGGGCA 360
TGGGTGGGTT CGTCCTCATG GCTACACAGT GAACCATGTG TTATTTTATT TTTCTAGACA 420
CTAAAGCTGA GGTGTCGGGA GGTGATGGTC CCTTGCTTGC AGGTGGCAGA GCTCAGGTTC 480
AAACCTGGAT CTTACTGCAC CTGGCTCGTT TGGGAGGCCT CCCTTGCTGG AATGCAGGTC 540
AGGGAGCCCC GATGCCCTTG GGCTGACTGC CCCACGTCCA TCACACCCAC TGAGGGCCGT 600
GGGGTGGGTG CAGGGCTTGT TCTGGGAGAT TCCAAGCTGA GGAAAGCAGG GCTGTCCGCC 660
AGCCTCCAGC TGGGTCACAG AAGAGGCTCA GGGCCTGTTC CCACTCCCCT CCCCCAGCCA 720
GCAGGGTCCA AAAGGATGTT GGGGGGGTGG TCCCCAGTCC GGCCTGCCCA CTCTAGGGAG 780
GGGCCCAGAT AACTTGCGTA GACGCCGGCC CTCCCGCCCC CAGCCTTCGC CATTGCCTTT 840
TGTCTGGCTA TCTTTCATGT ACAAGGGAGA AATTCAAGCC ACTCAGGAGG GTGTAACATG 900
AAAAGTCAGT CTCTCCTTCT CTCCGCACTG CCCGTGACCT GTGGTTTCTC AGGCACATAC 960
AAGCGCGCAC GCATAAATCT CTCCTCCAAC CTGCTGGGCT TCAAGTTATG CACGTTCACA 1020
CAATGGCAAA GGAGGGTGCG GATTGAAAAG TATGACTTGC TTCCCGGAGG CAGCACTGAA 1080
GTCACTTTAT TGTGTTTCCA GACAAGCCCC ATGAATGCAG TGTGCACTGC CCCTCCTCCC 1140
TCTGTCCCTT CCCCGCCCAT CTGTACACCT GTGGTGCGTA GGTTTTACAC CACTCTGTGC 1200
CTTACGTTGT GGCTCGATCA TTTAACATGT CAGTGTGTAC CGATGGAAAT TGATCTCTTT 1260
TAATTTGCCA CATCTTCATT TATTCATTCT TTGATTAATT GATGGATATT TAGGTTTTCT 1320
GCTTTGGGGG CATTCAGATC CAGGTGTATC TCTGCAAGTA GAGCTTGTAG CATACATAAG 1380
GCCCTGCAAA GGGATTTCTG GGCCGGAAGT TTTTGATCAG TTGCTCAGAC ATAGTTCTGA 1440
TGTGCTGGGG AAGTGCCCGT TCAGGGCCAT GGCTGCAGGG CTCCTGGACA CCCAGCTCCG 1500
GTGCTGGAGT GGGGTTGGGA TTCGCCCAGA GGCCAGGGCT GCGCCAGAGG AGCCCAGGGT 1560
GACCTCATGG TCCTCAGATA CCCGGGGCTG GGCAGCACAG TGGAACAGCT GCTCCAGAGC 1620
TTCTCCGAGG ACGACATCGG AGGATCCGAC TCAGGTTACG GCAGGAGAGG GAGGCCAGGC 1680
CGGGTTAGGG TTCTGGGGTT TGGGATTCTC TTCCGAGGCT GGCATTGATC TGTTGCTGAT 1740
GATGGTAACA GCAGCTGCTC TTGTTTATGA AGTACTTAAC ACCTCCAGCT CCCTCCATTA 1800
CCTAGGAATC CTCACTGCAG GGAGGGGTTT TCATCCCCAT TTTGTGCCTA TTTTATTTAT 1860
ATTATTTTAT TTTTTGAGGC AGGGTTTTGC TCTTGTTGCC CAGGCTGGAG TGCTATGGCA 1920
CGATTTCTGC TCACTGCAAC CTCTGCCTCC TGGGTTGAAG 1960
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