| Tag | Content |
|---|
EnhancerAtlas ID | HS060-23813 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr3:10239580-10242050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr3:10239716-10239728 | ACTAAAAATAGA | + | 6.27 | | MEF2B | MA0660.1 | chr3:10239716-10239728 | ACTAAAAATAGA | + | 6.32 | | MEF2C | MA0497.1 | chr3:10239714-10239729 | CTACTAAAAATAGAA | + | 6.57 | | ZNF263 | MA0528.1 | chr3:10240864-10240885 | AGTGGAGGAGGGGAGAGGAAG | + | 6.08 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_03544 | chr3:10240260-10240940 | Brain_Angular_Gyrus | | SE_05284 | chr3:10239556-10241713 | Brain_Cingulate_Gyrus | | SE_06271 | chr3:10239536-10241921 | Brain_Hippocampus_Middle | | SE_07281 | chr3:10239529-10241372 | Brain_Hippocampus_Middle_150 | | SE_08553 | chr3:10239744-10241777 | Brain_Inferior_Temporal_Lobe | | SE_10483 | chr3:10239552-10242463 | CD19_Primary | | SE_11117 | chr3:10230364-10244148 | CD20 | | SE_12182 | chr3:10239800-10241688 | CD3 | | SE_18222 | chr3:10230393-10242416 | CD4p_CD25-_CD45ROp_Memory | | SE_18887 | chr3:10239325-10242218 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19527 | chr3:10239586-10241934 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20302 | chr3:10239719-10242481 | CD56 | | SE_22972 | chr3:10239783-10241915 | CD8_primiary | | SE_27300 | chr3:10239815-10241654 | Esophagus | | SE_35045 | chr3:10239193-10242641 | HeLa | | SE_36305 | chr3:10239752-10241604 | HMEC | | SE_38379 | chr3:10239866-10241762 | HUVEC | | SE_46480 | chr3:10239746-10241594 | Osteoblasts | | SE_55870 | chr3:10239757-10241715 | u87 | | SE_55870 | chr3:10241720-10242605 | u87 | | SE_58615 | chr3:10208482-10269048 | Ly1 | | SE_62498 | chr3:10211834-10316085 | Tonsil | | SE_64685 | chr3:10239754-10241685 | NHEK | | SE_67695 | chr3:10239757-10241715 | u87 | | SE_67695 | chr3:10241720-10242605 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr3 | 10239722 | 10241621 | | chr3 | 10239937 | 10241585 | | chr3 | 10241844 | 10241924 | | chr3 | 10240437 | 10240684 | | chr3 | 10240691 | 10241307 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I010188 | chr3 | 10230458 | 10242599 |
|
Enhancer Sequence | ACACAAGGAA GAAGCCACTC AGGCCGGGCG CAGTGGCTCA CGCCTGTAAT CCCAGCACTT 60
TGGGAGGCTG AGGAGGGCGG ATCATGACGT CAGGAGATCG AGACCATCCT GGCTAACACA 120
GTGAAACCCT GTCTCTACTA AAAATAGAAA AAATTAGCCG GGCGTGCTGG TGGGCGCCTG 180
TAGTCCCAGC TACACGGGAG GCTGAGGCAG GAGAATGGCG TGAGCCCGAG AATCGGAGCT 240
TGCAGTGAGC CAAGATCACA CCACTGCACT CCAGCCTGGG CGACAGAGCG AGACTCCGTC 300
TCAAAAAACA AAACAAAACA AAACAAAACG AAAATTTATT TAAAATGTCA GTGACAGTAA 360
AGAAAACACA AGGACGAAGC CACTCATCAC CCCCCGACAT TCAGCCTTGT TGTTATTTTT 420
GTGCATTCCC GATGTCTCCC CAACTCCTCC CACCCTGGGG AAGTCAGTGA TCACCCCTTT 480
GTTCCTGTTT GTCTGGGGAT TGGGGCGTCT GCCCCTGGGG GAATTGGGGC TGGTGGTGGC 540
AGTGATGGCA GTGGTGTTTC AATAGTTCTG CCCTAGCTGG GTGGGAGACA GTGAAACCAG 600
TCCCAGGTTT GACTGTTGTT GGCTGTTTTA CTTGACACAA GTCATTTCAC TTATCTGAGC 660
CTCAATATAC TCAAAAATAA AATGCAGATA AACCTATGAA CTACCAGAGA TTGTTGTGAA 720
AATTAAATAA ATATGCACGG TGCCATACCA GTGTGGTGCT ATGCAAATTT AGGTCCTATT 780
ATTTTAGTTC AAAAGCTTGG GTTTGAAAAG TGAGGTCCCA GGGTAACAAT TGGTTTTGTT 840
TAGAGAGGCA CAGTTGACCA GTTCAAAGAA ATGTTGCTGG AGATGTTTTG TCCCAGCCCT 900
ACCTGGGACA TCTGTTGTGA CATCCCCTGT GTCATGCTTT ATGTCATGCT CTGTGTGACA 960
TCAAGCGAGT CAGCAGCCCT TCCTGGGACT TCAGTGCCCC AGTTTTTGTC ATTCTCAAAC 1020
ATGAGTCTAT CCCAAACCAC CAGAGAATGA GGGACTTGAA TGCAGGGCTA TAGCATCAGG 1080
TTTTATCTGG GAGGCAATGG GGAGACAGAA AGATTCAGGC TAAGGAGTGT GGACATTATC 1140
TAGGCAATGG GGAGCCCCAT AAAGGCTTCA AGCAGGGAAG TGACGAGGCC AGATGTATAC 1200
TTTGGTAAGA AGTAGCCTGG CAAGGGTGTG GAGGCTGCCT GAGCTGGCGG CAGGGCCCAG 1260
CCAGAAGGGA TAAGATCAGG GCCCAGTGGA GGAGGGGAGA GGAAGCTGTT TCACAGAGCA 1320
GCTCTGAGAA GCTGGCTGGA AGCTGAGGTT GACACACCCT CGAAGCACCT TTGGGGTTTC 1380
CCAAGTTGAT GTAAAAAGGA AATGATTACC CTCGAGAAGG CAGGGGAGTT CTTCGGCCAG 1440
TCCTGCGTGC CTTTGGCATG TGATCTTAGC AAGTCATTTA ACCTGCTCAG GCCTCAGTTT 1500
CCTCATCTCT GAACAGGGAT GAGAAGCAGA GATGTTGTGA GGATTCATGT CTGTGCAGCT 1560
GGGCCTGGGC CTGGTACAGC CCGTCCTCAG TGGCCATGGC TGCTGTTTTA GGATTCTCAT 1620
CCATCAAGTG GGAAGGATGC GTTTGTCTCC ACTGCGTGAA AGGGAGGTTG TAGGACAGCC 1680
AGAACTTTGA TCCCTAGGGG CTGGAGTGGG AGCTTAGAGG GATGGTGTCT TTGACCCGCT 1740
CACGTGTTCA GGGAAATGTG CAGTCTACAG CGCCCATTCC CATCTCTACT CTCCTTTCCC 1800
ACATGACACC CCAGCGGGAG GCAAACGGAC GCCATTATCA CCTCCGTTTT ATAGGTGAGG 1860
GAAGGGAGAC CGAGAGGAGG AAGGTGACTT GTTGGAGGTC ACACAGCTGG TTGGGTGGAA 1920
GCAGGTGTAT GTGACTTAGC ACGTCAGAGC TCCACCTTCA CCAGGACTGC CATGTTCAGC 1980
CACTGCTCTT TTTTTTTTTT TTTTTTTTTG AGACAGAGTC TTGCTCTGTC GCTCAGGCTG 2040
GAGTGTAGTG GTGCGATCTT GGCTCACTGC AAGCTCCGCC TCCCCGGTTC AAGTGATTCT 2100
CCTGCCTCAG CCTCCCAAGT AGCTGAGACT ACAGCCGTGT GCCACCATGC CCAACTAATT 2160
TTTGTATTTT TAGTAGAGAT GGGGTTTCAC CATGTTGGCC AGGCTGGTCT CGAACTCCTG 2220
ACCTCAGGCA GTCCACCCAC CTCGGCCTCC CAAAGTGCTG GGATTACAGG TGTGAGCCAC 2280
CGCGCCTGGT CTACCGCATT TTACAGATGG GGAGGCCGGG GCCAGAAAGG GAAAGACCCT 2340
CCCGCCCTGC AACACCATGC ATTTGTGGCA GAGCCAGAAT TAGAACCCAG GTCTCTGACT 2400
TCCAGAACCA GTCTCTCAAT GGCTACCCCA CTTCATGGAA TAGTAATAAC TTTCTTTCCA 2460
CCTTGTTTTC 2470
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