Tag | Content |
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EnhancerAtlas ID | HS007-11176 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr3:42084200-42085980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr3:42084920-42084935 | TGACCCCTGCCCTCC | - | 6.26 | RREB1 | MA0073.1 | chr3:42085253-42085273 | ACCCACCCCACCCCCCCGCC | + | 6.5 | ZNF263 | MA0528.1 | chr3:42084714-42084735 | CCCCTCTTGCCCTCCTTCTCC | - | 6.13 | ZNF263 | MA0528.1 | chr3:42084861-42084882 | ACCCTCTTCTTTCCCTCCTCC | - | 6.85 | ZNF740 | MA0753.2 | chr3:42085107-42085120 | GGGGGGGGGGCGG | - | 6.64 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00063 | chr3:42083844-42085337 | Adipose_Nuclei | SE_00063 | chr3:42085462-42086940 | Adipose_Nuclei | SE_01171 | chr3:42084456-42085293 | Adrenal_Gland | SE_01796 | chr3:42084082-42085215 | Aorta | SE_01796 | chr3:42085585-42086306 | Aorta | SE_02512 | chr3:42084169-42086780 | Astrocytes | SE_23272 | chr3:42084482-42084941 | Colon_Crypt_1 | SE_25861 | chr3:42084036-42085319 | Duodenum_Smooth_Muscle | SE_26989 | chr3:42084415-42085612 | Esophagus | SE_29565 | chr3:42082891-42086556 | Fetal_Muscle | SE_36966 | chr3:42083441-42087043 | HSMMtube | SE_38230 | chr3:42083593-42087657 | HUVEC | SE_40683 | chr3:42083847-42086405 | Left_Ventricle | SE_42248 | chr3:42084050-42085282 | Lung | SE_44918 | chr3:42084214-42085341 | NHLF | SE_45733 | chr3:42083774-42087928 | Osteoblasts | SE_48185 | chr3:42083909-42085895 | Psoas_Muscle | SE_48670 | chr3:42084049-42085365 | Right_Atrium | SE_49555 | chr3:42084540-42085234 | Right_Ventricle | SE_50309 | chr3:42084420-42085321 | Sigmoid_Colon | SE_51166 | chr3:42083485-42088240 | Skeletal_Muscle | SE_51885 | chr3:42084259-42085172 | Skeletal_Muscle_Myoblast | SE_51885 | chr3:42085748-42086527 | Skeletal_Muscle_Myoblast | SE_52625 | chr3:42084189-42085236 | Small_Intestine | SE_53513 | chr3:42084267-42085413 | Spleen | SE_54717 | chr3:42084158-42085172 | Stomach_Smooth_Muscle | SE_62800 | chr3:42053253-42125059 | Tonsil | SE_63663 | chr3:42084221-42085236 | HSMM | SE_65769 | chr3:42084218-42085429 | Pancreatic_islets | SE_65769 | chr3:42085552-42086516 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 42084224 | 42085413 | chr3 | 42085864 | 42085949 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I042041 | chr3 | 42083046 | 42088343 |
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Enhancer Sequence | AGTAGAAATT TCTTCTGCTT GCAAATTGTT TTTCAGTGAA CCCATGAAAA CGATTGCTTC 60 ACAGTGTATG CTCCAGGATG GAATACAGTT CTTAATGTAG AGGGTGCACT AGCTCTTCCT 120 CTCTCTGGGG CGGGTCATCT GTTGTACTCA CTGCTCTGAT TACATTCTCT AATATTTAAG 180 TAGACCATGA CCTGTCATGG TCTGGACGTG TGGCTAATTA TACTTATCTC CTCATCTCGT 240 CTTTAAAAAA GAATGATCTC AGATTCTTAT TACCAAAGGA CGTTGGCCTC CTTTGTAGAG 300 AATACTTTGG GAAGGATCCT TCTGTGGAGT TTGATCCTGG GGACTCTGAC TTTAGAGTTC 360 TTGCTGATCT TTCCTCTCCC TTTAAGGGTA AGGATTAGTA TATCTGCAGA CATCTCCAAG 420 CTTAAGCTTT GTTATTGTGG GCTTATGGGC AGCAGCTTAG CAACCATTTC AAGGCACTCA 480 GCTGTCTCAT GGGTCTGTCT CTGCTTGTCA CTGTCCCCTC TTGCCCTCCT TCTCCTCCCT 540 CTCACATTGC CCGTTCCCGT TCTTTCTTCC CTTGTCCTCT TACCCGTCTC CTCCTTTTTG 600 TCCAGCATTC CTCTCTTTCC TATCCCCTCC CCGACTCACA CTCCCTCTTG CTGCTTCCCT 660 CACCCTCTTC TTTCCCTCCT CCTTGTCTCT TTGCCTTTTC TCCTCCTAGT CCCCTCCTCC 720 TGACCCCTGC CCTCCCTCTC TCCTTTTGTC TTGGGAATCC TTTGTCCCTG CTCTGACCTC 780 ATCCCCTCCA CCCCTACCCC CAGCCCTGTG AGCAGACCTC TCCAGCTTCT GATGGATGTT 840 GTCTTTGGCT TTTCGCCAGT GTGTTTTTCC AGCTCCAGAC CCTGTGTCTT GTTTTCTCCA 900 TGGAGCTGGG GGGGGGGCGG GGGGAGTAAA GGGGATCCTG GTTTTCATGG TCTCAGGCAG 960 GCTGTGTCTG CAGCGTTTGG CCATTTCTGA GCCAGTCCCT GGCTTTGTTT CTTGGTATTT 1020 CCGGTTCTCC CAGTGGCCTG TTAGGATGAC AGGACCCACC CCACCCCCCC GCCACCCCAA 1080 CTCCCCAGAG GGGGCACAGG TTTGAAAGAG GACCATGCTT TGGTCTCTTA AGAGCACTTG 1140 ATTACTTGAC AGACGGCCTT CTATACCTTT CAGTTGGCAG GAAGCCACCT TTTTTTTTAA 1200 AATTACTTTA AAATTTATTA TAAATAAAAC AAAATTATTT CTGTGGTCAA GTTTACTATT 1260 TTGAAAATGG GAACTCATGT GTTTGTCATC TGCTGGTGGG CCCTGGGCCT GGGCAGAAGC 1320 CCAGCTTTCA GGTGGCCCAA GGCACTGGAT TGTTTGATTT TGGATCTTAA AACTGATTTT 1380 GGAATTTTAA ATCAATTTTT CAGTTCTGCC TCAGTGTCCA GTCTGTCCTT TTCATCCCCA 1440 TCTGCTTTTC ATTTTATTTA TTTATTTTTT GAAACAGGGT CTTGCTCTGT CGCCCAGGCT 1500 GGAGTGCAGT GGCACAATCA CAGCTCACTG CAACCTCTGC CTGTCAGGCT CAGGCAATCC 1560 TCCCACCTCA ACCTCCCTAG TAGCTGGAAC CACAGGTGCA CACCACCACA CTTGGCTAAT 1620 TTTTTGTATT CTTGGTAGAG ACAGGGTTTC ACCGTGCTAC CCGGGCTGGT CTCGAACTCC 1680 TGAGCTCAAG AGATCCACTT GCCTCGGTCT CCCAAAGTGC TGGGAATACA GAAGTGAGCC 1740 ATTGTGCCTA GCCCATTGTA TTTTCTTGAA GGCCATTTGA 1780
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