Tag | Content |
---|
EnhancerAtlas ID | HS116-22899 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr3:10233000-10235170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr3:10233584-10233598 | AAAGAATGAGTCAT | + | 6.6 | RELA | MA0107.1 | chr3:10233977-10233987 | GGGAATTTCC | + | 6.02 | RREB1 | MA0073.1 | chr3:10233730-10233750 | TGTGTGTGTGTGTGTTGTGT | - | 6.19 |
|
| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_01374 | chr3:10232903-10233512 | Adrenal_Gland | SE_01374 | chr3:10233588-10237950 | Adrenal_Gland | SE_02168 | chr3:10232890-10237812 | Aorta | SE_03544 | chr3:10232926-10234465 | Brain_Angular_Gyrus | SE_03544 | chr3:10234523-10235075 | Brain_Angular_Gyrus | SE_05284 | chr3:10230421-10238972 | Brain_Cingulate_Gyrus | SE_06271 | chr3:10230310-10239221 | Brain_Hippocampus_Middle | SE_07281 | chr3:10230345-10238980 | Brain_Hippocampus_Middle_150 | SE_08553 | chr3:10230394-10238941 | Brain_Inferior_Temporal_Lobe | SE_10483 | chr3:10232905-10238935 | CD19_Primary | SE_11117 | chr3:10230364-10244148 | CD20 | SE_12182 | chr3:10233126-10238474 | CD3 | SE_18222 | chr3:10230393-10242416 | CD4p_CD25-_CD45ROp_Memory | SE_18887 | chr3:10230456-10239154 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19527 | chr3:10232850-10237954 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20302 | chr3:10232846-10239394 | CD56 | SE_22972 | chr3:10232902-10238955 | CD8_primiary | SE_27300 | chr3:10232887-10237905 | Esophagus | SE_35045 | chr3:10230429-10236765 | HeLa | SE_36305 | chr3:10230416-10237861 | HMEC | SE_38379 | chr3:10230299-10236156 | HUVEC | SE_46480 | chr3:10232852-10239588 | Osteoblasts | SE_55870 | chr3:10232869-10239613 | u87 | SE_58615 | chr3:10208482-10269048 | Ly1 | SE_62498 | chr3:10211834-10316085 | Tonsil | SE_64685 | chr3:10232624-10237158 | NHEK | SE_67695 | chr3:10232869-10239613 | u87 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 10233010 | 10234358 | chr3 | 10234749 | 10235085 | chr3 | 10233695 | 10234220 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH03I010188 | chr3 | 10230458 | 10242599 |
|
Enhancer Sequence | TAGAACCAGT CGTGACGCCC AGCCTAATTG CTAAGGAGGC AGGAGTATGA GACAGAGCAG 60 ATGGTTATTT GGTAAGTACT CTCTCAGCTA CAGGTTACCT CAGTTCCAGG GCGCTTACAG 120 TAAGGTTCTG CCTAACTGTG GCCTACAAGG CCCTGCATGG TCTACCTTTG CCCGGCTCTT 180 CAACCTCACC TCTACCACTT TCCCCCTCAG TCATTCCCCT CAGCCACTAC GGTCATCCTT 240 CACTTGCGGG GATATGCCAA GTGTTTGCTG CCTAAGGACC TTTGCACACG TGTTCCCTCT 300 CCTTGGAATG CTGTCTCTCC CCAGCTTCCC TACATTCTTC CATGCTAGTC CTTTTCATCC 360 TCTGGGTGTC TGCATATGTG GCCCCTTCTC ATGGCAGCTT TTCCTGGCCA GCCTATGGAA 420 GTAGGTCCAT CAGGCACCCC TCCCTCGAGT TTGTTTTCAG CATAGAGCAC CTCCCAGTTT 480 ATAATTAGAT GTCTTTTATT TAACTAGCTT AATGTCAGTA TTACGGCAGT TTTGATAAAG 540 GATTCCCCAT TCCCTAACAC AAAATGAATG AATGAATGAA TGAGAAAGAA TGAGTCATTT 600 CAGCAGCAGG TGGAGTACAA GTTCAGTGGA GAACCAGGGA TCGCACAATT AGGAAGGCAG 660 GCTGTGCTCT CAGGTTTGCC TCATTTCAGG TCTAGCTTGA GTTGGGAGTG TGTGTGTGTG 720 TGTGTGTGTG TGTGTGTGTG TGTGTTGTGT GTTGTGTGTG ACTGTGTATG GCCTGGAGGG 780 CCAAACCCAG GGATTAGGAG GGAAAGGAAA AGAGAGGGCG CGGAAAGCTG TGTTTGTCCC 840 TGATAGAGCC AGCTGGCACG AGGGTGCTTT AGTTATAGCT GAATCACTTT TGTTTGTTCT 900 GGAAGGGATC TATTCTGGCC ACATGAGTCA GCCTAAGAAC AAATTACTGT GTAGTTTGAC 960 GGGCGTGAAG GGTTGGGGGG AATTTCCAGA GTGTGCTCAC CCAGGAAAGA CCTTGTTGCC 1020 AGCTCTGAGT CCCCTCTGCT CCAACAGCTC CTGGATTTGC CACCGTGTGA AATGTTCTCA 1080 GGCAGCTAGT GTGACGGCCC AGGCCCCGTC AGCCAAAGGC CCAGCACCCA TAAACATCCT 1140 TTAGTCCTTT CTCCTGAAGG AACTGGGCCA TAAACAAGCA CATAATAAAT AAATCTGCAT 1200 TCTAGGCTTC GCTTTCTTCA GATATAAGAC AACTACCTTA TACTTGGTAG CAATTATCCC 1260 CCAGAGCTGT TACCTGAATT AAATAGGCCA CAGATATGGG CAAGAACTTA GGAAAAAAAG 1320 CCTGACCTAG AGTTAGAGTG GTCATTATAA TAACAGTAGT AGGAGGCCAA GGCGGACGGA 1380 TCACCTGAGG TCAGGAGTTC GAGACCAGCC TGGCCAATAT GGCAAAACCC CGTCTCTACT 1440 AAAAATACAA AAATTAGCCG GGCGTGATGG TGTCTGCCTG TAATCCCAGC TACTCGGGAG 1500 GGTGAGGTAG GACAATCGCT TGAACCCAGG AGGCAGAAGT TGTAATGAGC AGAGATCGTG 1560 CCACTGTACT CCAGCCTGGG CAACAGAGCG AGACTATAGC AAATGATGGT AGCTTAGATC 1620 TGCTGGGTGT TAATTTTTTT ATCCTCATGG CTGGTCTCGG GTCGGGGGTC CACTTCCACA 1680 TCTCATTTGT CGGATGAGGA AGCCAAGGCT TAGGAGGATC CCCCTGCTGG TGAGCCTGAC 1740 TGCAGGACAC ACTCCAGACT GCGGGAGTTC ATTTGCCTTC CGTGGCATCA GTGATTCATG 1800 CTCATTAGGA AGAGCACAGG CATTCCGAAA ACAAATCAGA GAGAAAAAGA AATCATGCCT 1860 GGCAACCAGC TCTGGTGAAC CATGACAGGG GCACAGAGAA GCGCTTCTGC CCCTCCCCCA 1920 TTTCCTCCTT GTATCTGGGA CTCAGCCCTC ATCACTGTGG GTTCTCAGCC TCAGCAAGGC 1980 AGCTTTCACG GATATCCAGA TTCCAGGCTG GGTGCAGTGG CTCACACCTG TAATCCCAGA 2040 ACTTTGGGAG GCCAAGGCAG GTAGATTGCT TGAGCCCAGG AGTTTGAGAT CAGCTTGCGC 2100 AATATGGCAA AACCCTGTCT CTACCAAAAA AAAACAAAAA CAAAAACAAA AACAAAATTA 2160 GCCTGGCGTG 2170
|