| Tag | Content |
|---|
EnhancerAtlas ID | HS108-26218 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr21:45615420-45617600 |
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 | CCAAATAGAA ATAAAACCTG GCTGTCTGGT CCTGATCCAC TCACAGAAGT GGCGTAAACA 60
CCTTATTTAT GATCTGGGAC ATTCAACACC ATCTTATAAA AGATTCATAG AATACACATT 120
CACACACCCA CAAAAATCAA GAGAGCAGAT TTTCCAAAAA TAGGTGCAAG AAAGATCCAA 180
CTTCCAGGAT AAAATTTTAG AACCAACATT TCCATTAGCA AAAGCGGTCT TGTCTAAAAC 240
TCTACCGACC GCGCTAAAAT CCCATTCAAA ACAGAGCTCT GGTTACGTAG ATCGTGATCA 300
ATAATGAGAA ACTGTGAGGC GTCCCCGTGG GATCTGACAC TTCCTAGGGG AGCTTCTCTC 360
CACTGGTAAT AAAGATATAA TTAGGAATTT CAACTACCTG TGATTTTGCC AACTTACGGC 420
ATTTGTTGAG AATTTCGGTC CCTGTGTTTA TGCACACACC TTTCAACCTT AGATTTGACG 480
GTGATGGGTT AGTAAATGTC AATTCTAAAG TGGTCGTTTT CAACCAGGGG CAATTTTACC 540
CCTCAGGGGA CACTGGCAGT GTCTGGAGAC ATGTTTGGTT GTCATGACTT GGGGCAGAGG 600
TGCCACGGGC ACCTGGAGGG TGGAGGCCGG GGTGCGGCTC AATACCCTAA CCACACAGGA 660
TGGCCCCAGG ACAAAGATGC CCCTGGTGCT GAGAGCAGGG CCCTGTTCTA AGAGATGGGT 720
GGCTGGAGCC TGGCTGGAGG GCACTAGTGG CACTCTGGGC TGGTCTCCCA GGGCCCCATC 780
TGCCAGGTCG GGGGCCCACG TGGGCCTGCA GGATGTGCGT GCTTCTCTGC TGTTGAGATT 840
GCATCAGCAC AACAGCCACA GCCGTGACAC GGGGGCAGGC ACCTCAGTGA CGCCAGAGTC 900
GGGGCGGGAG GTGTGGAGAT CTGGGCTTGC TTCCTCTTTT CAGTCCCAGG ACAGCTCCTC 960
TTTGGCTGTG GGAGGCCCAG CTTCAGCCTT GTCTGTGGCT TCCTGGTGGG AGGACACAGG 1020
CCTTGAGGGA CGTTTGTCCG AGACGGTCCT CATCCTACTG GTAGGGACAC AGAGCACCTG 1080
TTCCTCTGGC CCCTCCAGGA GCAAGACACA TGCACTGCTG AGGCCTTGGA AGCCTACACA 1140
GGTTTATCAC CCACGGCCAG ACCTGTCTGT CAGGGAGCAG GTGGGGTCAT CCTGCCCTGA 1200
AGCACCGATG AGCTGATCCC GGTCATGCAG AGTGGGTGGG GACCTCTTGG CTGGGCCTGT 1260
TCATGTAGCA CACACGGCTT TGCTGCCCAT AGAATCCAGG GCCCCCAGTG TGAGCACCAC 1320
TCTCCATCCC TGAGGCCGAG CCTTACCCTG GAGGCAGCCT CAGGTGAGAT GCCCCTAATG 1380
GAGCCACCTG GCAATGGACC GCTCTCAGGT CCTTCAGCTC GGTGCACTCA CCCGGGAGCC 1440
CTGCGTTCTG TCCTGGGGTA GAGGCTCAGG GTTGGTTTGA AGCCATATAG TCAGCTCCCA 1500
GAGTCACAGA AACGTCCAAG GAAGAAAACT GTCCGATTAC AGACTTTTAA AATTCATTCA 1560
TAGTTTAATC AAGAGAACTT GCTGTTCCTT CCTCAAATTT CCTAGAATTG GTCTTCTCAT 1620
AATCACCACC TAGGGCACAG CTGTGGCCGA GGCTCCCATG ATGAAGCGTC TGTGTCAGCG 1680
CTGACGAGGT CTGCCGAGGA CGCGTTTCTC TCTGCAGCCC GGCACCAGTC TCAAGGCCAT 1740
CGGCTCCGAC AGCGTCACCT CCTGGGACCT TCCCTTCATG TATGGTCCCA GCGGCATGCG 1800
GGCCTGGTGG AGGAGGTCCT GGCCTGCCGC CCAGGGATGG CCGGTCCAGG CGCAGGGCCG 1860
ATTGTCCACT TCTGGCCCCT GAGGTACCGG GAGGGCTGGT GAGCAGCATG TCTCGCTCTG 1920
AGACCGGCCA GGCTGCTGGG GCAGGCATCT GATGTACAGT AGTTCCCACA CGTGGCAATG 1980
TCACCAGCAA GAGCCACGTA TGATAAATTC AGGCCGTCCA CCGTGGCAAC ACTGGGAAGG 2040
CTGATTCTGT AGGAAAGGAT TGGCCTTGGG CCATCACTGT TCAAAGAAGA AGAAATCCCT 2100
GGATCACTGT CTGATCCAAC TCCAGACAGA CACTCCACAC AGGATTCCTC CTGGGGATCA 2160
CGGCTCTTCT CTTGGCGGAG 2180
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