| Tag | Content |
|---|
EnhancerAtlas ID | HS187-15928 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr21:45615360-45617620 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr21:45616347-45616361 | TGCTTCCTCTTTTC | - | 6 | | SPIC | MA0687.1 | chr21:45616347-45616361 | TGCTTCCTCTTTTC | - | 6.1 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_00694 | chr21:45616149-45617521 | Adipose_Nuclei | | SE_03880 | chr21:45616016-45617515 | Brain_Anterior_Caudate | | SE_04775 | chr21:45609944-45617953 | Brain_Cingulate_Gyrus | | SE_05779 | chr21:45610164-45618120 | Brain_Hippocampus_Middle | | SE_06690 | chr21:45610194-45617897 | Brain_Hippocampus_Middle_150 | | SE_07737 | chr21:45615485-45617603 | Brain_Inferior_Temporal_Lobe | | SE_10305 | chr21:45615103-45617503 | CD19_Primary | | SE_11616 | chr21:45614519-45618143 | CD20 | | SE_24239 | chr21:45615918-45616296 | Colon_Crypt_2 | | SE_24239 | chr21:45616358-45616947 | Colon_Crypt_2 | | SE_30176 | chr21:45612703-45617986 | Fetal_Muscle | | SE_31647 | chr21:45615831-45617002 | Gastric | | SE_31647 | chr21:45617022-45617833 | Gastric | | SE_40890 | chr21:45615577-45618069 | Left_Ventricle | | SE_42286 | chr21:45615697-45617796 | Lung | | SE_48538 | chr21:45614456-45617946 | Psoas_Muscle | | SE_50113 | chr21:45615772-45617519 | Sigmoid_Colon | | SE_51445 | chr21:45609930-45618288 | Skeletal_Muscle | | SE_52463 | chr21:45615642-45617687 | Small_Intestine | | SE_59125 | chr21:45557380-45640832 | Ly3 | | SE_61237 | chr21:45557180-45641526 | HBL1 | | SE_61527 | chr21:45545883-45641600 | Toledo | | SE_62281 | chr21:45556124-45641130 | Tonsil | | SE_65639 | chr21:45615968-45617001 | Pancreatic_islets | | SE_65639 | chr21:45617003-45617940 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr21 | 45615654 | 45615733 | | chr21 | 45615635 | 45617233 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH21I005064 | chr21 | 45615830 | 45617229 | | GH21I044192 | chr21 | 45612024 | 45617843 |
|
Enhancer Sequence | AGATGCCTCT GTCAAGAAGG AGCCACGAGT TGGCTTTCAT GGAATGGGTG CTCTTGGTGG 60
CCAAATAGAA ATAAAACCTG GCTGTCTGGT CCTGATCCAC TCACAGAAGT GGCGTAAACA 120
CCTTATTTAT GATCTGGGAC ATTCAACACC ATCTTATAAA AGATTCATAG AATACACATT 180
CACACACCCA CAAAAATCAA GAGAGCAGAT TTTCCAAAAA TAGGTGCAAG AAAGATCCAA 240
CTTCCAGGAT AAAATTTTAG AACCAACATT TCCATTAGCA AAAGCGGTCT TGTCTAAAAC 300
TCTACCGACC GCGCTAAAAT CCCATTCAAA ACAGAGCTCT GGTTACGTAG ATCGTGATCA 360
ATAATGAGAA ACTGTGAGGC GTCCCCGTGG GATCTGACAC TTCCTAGGGG AGCTTCTCTC 420
CACTGGTAAT AAAGATATAA TTAGGAATTT CAACTACCTG TGATTTTGCC AACTTACGGC 480
ATTTGTTGAG AATTTCGGTC CCTGTGTTTA TGCACACACC TTTCAACCTT AGATTTGACG 540
GTGATGGGTT AGTAAATGTC AATTCTAAAG TGGTCGTTTT CAACCAGGGG CAATTTTACC 600
CCTCAGGGGA CACTGGCAGT GTCTGGAGAC ATGTTTGGTT GTCATGACTT GGGGCAGAGG 660
TGCCACGGGC ACCTGGAGGG TGGAGGCCGG GGTGCGGCTC AATACCCTAA CCACACAGGA 720
TGGCCCCAGG ACAAAGATGC CCCTGGTGCT GAGAGCAGGG CCCTGTTCTA AGAGATGGGT 780
GGCTGGAGCC TGGCTGGAGG GCACTAGTGG CACTCTGGGC TGGTCTCCCA GGGCCCCATC 840
TGCCAGGTCG GGGGCCCACG TGGGCCTGCA GGATGTGCGT GCTTCTCTGC TGTTGAGATT 900
GCATCAGCAC AACAGCCACA GCCGTGACAC GGGGGCAGGC ACCTCAGTGA CGCCAGAGTC 960
GGGGCGGGAG GTGTGGAGAT CTGGGCTTGC TTCCTCTTTT CAGTCCCAGG ACAGCTCCTC 1020
TTTGGCTGTG GGAGGCCCAG CTTCAGCCTT GTCTGTGGCT TCCTGGTGGG AGGACACAGG 1080
CCTTGAGGGA CGTTTGTCCG AGACGGTCCT CATCCTACTG GTAGGGACAC AGAGCACCTG 1140
TTCCTCTGGC CCCTCCAGGA GCAAGACACA TGCACTGCTG AGGCCTTGGA AGCCTACACA 1200
GGTTTATCAC CCACGGCCAG ACCTGTCTGT CAGGGAGCAG GTGGGGTCAT CCTGCCCTGA 1260
AGCACCGATG AGCTGATCCC GGTCATGCAG AGTGGGTGGG GACCTCTTGG CTGGGCCTGT 1320
TCATGTAGCA CACACGGCTT TGCTGCCCAT AGAATCCAGG GCCCCCAGTG TGAGCACCAC 1380
TCTCCATCCC TGAGGCCGAG CCTTACCCTG GAGGCAGCCT CAGGTGAGAT GCCCCTAATG 1440
GAGCCACCTG GCAATGGACC GCTCTCAGGT CCTTCAGCTC GGTGCACTCA CCCGGGAGCC 1500
CTGCGTTCTG TCCTGGGGTA GAGGCTCAGG GTTGGTTTGA AGCCATATAG TCAGCTCCCA 1560
GAGTCACAGA AACGTCCAAG GAAGAAAACT GTCCGATTAC AGACTTTTAA AATTCATTCA 1620
TAGTTTAATC AAGAGAACTT GCTGTTCCTT CCTCAAATTT CCTAGAATTG GTCTTCTCAT 1680
AATCACCACC TAGGGCACAG CTGTGGCCGA GGCTCCCATG ATGAAGCGTC TGTGTCAGCG 1740
CTGACGAGGT CTGCCGAGGA CGCGTTTCTC TCTGCAGCCC GGCACCAGTC TCAAGGCCAT 1800
CGGCTCCGAC AGCGTCACCT CCTGGGACCT TCCCTTCATG TATGGTCCCA GCGGCATGCG 1860
GGCCTGGTGG AGGAGGTCCT GGCCTGCCGC CCAGGGATGG CCGGTCCAGG CGCAGGGCCG 1920
ATTGTCCACT TCTGGCCCCT GAGGTACCGG GAGGGCTGGT GAGCAGCATG TCTCGCTCTG 1980
AGACCGGCCA GGCTGCTGGG GCAGGCATCT GATGTACAGT AGTTCCCACA CGTGGCAATG 2040
TCACCAGCAA GAGCCACGTA TGATAAATTC AGGCCGTCCA CCGTGGCAAC ACTGGGAAGG 2100
CTGATTCTGT AGGAAAGGAT TGGCCTTGGG CCATCACTGT TCAAAGAAGA AGAAATCCCT 2160
GGATCACTGT CTGATCCAAC TCCAGACAGA CACTCCACAC AGGATTCCTC CTGGGGATCA 2220
CGGCTCTTCT CTTGGCGGAG AAGAAGGAGG GAGAATGAGC 2260
|
