| Tag | Content |
|---|
EnhancerAtlas ID | HS104-05143 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:204445740-204448440 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:204448382-204448403 | TCCTCCCCTCTTCCCTCACCC | - | 6.43 | | ZNF263 | MA0528.1 | chr1:204448378-204448399 | TTCCTCCTCCCCTCTTCCCTC | - | 6 |
|
| | Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
| SE_00064 | chr1:204447165-204449222 | Adipose_Nuclei | | SE_01898 | chr1:204446732-204449955 | Aorta | | SE_03188 | chr1:204445701-204449764 | Brain_Angular_Gyrus | | SE_03975 | chr1:204443311-204451730 | Brain_Anterior_Caudate | | SE_04850 | chr1:204441602-204452008 | Brain_Cingulate_Gyrus | | SE_05834 | chr1:204441572-204454041 | Brain_Hippocampus_Middle | | SE_06778 | chr1:204441694-204452486 | Brain_Hippocampus_Middle_150 | | SE_07775 | chr1:204441566-204452208 | Brain_Inferior_Temporal_Lobe | | SE_10905 | chr1:204440571-204455347 | CD20 | | SE_24481 | chr1:204446396-204446926 | Colon_Crypt_2 | | SE_24481 | chr1:204447117-204447620 | Colon_Crypt_2 | | SE_24481 | chr1:204447850-204448210 | Colon_Crypt_2 | | SE_25125 | chr1:204446211-204447705 | Colon_Crypt_3 | | SE_25125 | chr1:204447777-204450200 | Colon_Crypt_3 | | SE_25573 | chr1:204447782-204451557 | DND41 | | SE_26688 | chr1:204446142-204447580 | Esophagus | | SE_26688 | chr1:204447747-204450316 | Esophagus | | SE_31610 | chr1:204446257-204447742 | Gastric | | SE_31610 | chr1:204447799-204450438 | Gastric | | SE_37407 | chr1:204442628-204450806 | HSMMtube | | SE_42225 | chr1:204446187-204447730 | Lung | | SE_42225 | chr1:204447736-204452375 | Lung | | SE_49909 | chr1:204444472-204450053 | RPMI-8402 | | SE_50149 | chr1:204447708-204450485 | Sigmoid_Colon | | SE_52421 | chr1:204446127-204447357 | Small_Intestine | | SE_52421 | chr1:204447689-204449720 | Small_Intestine | | SE_58430 | chr1:204415099-204506026 | Ly1 | | SE_59794 | chr1:204415680-204491493 | Ly4 | | SE_61475 | chr1:204430067-204500813 | Toledo | | SE_62377 | chr1:204415291-204492168 | Tonsil | | SE_65868 | chr1:204446405-204446982 | Pancreatic_islets | | SE_65868 | chr1:204448014-204448665 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH01I204477 | chr1 | 204446360 | 204447003 | | GH01I204478 | chr1 | 204447118 | 204447620 | | GH01I204479 | chr1 | 204447921 | 204451603 |
|
Enhancer Sequence | GATTCTGTAT AAAAACAAAT AGCCATGTCG GTCCCTTGAA AGAGGAAGGG TAGATCAGGG 60
CCTGCGTCTC TGCTACTCTG CAGCCCATCC AGGGAGAGAT GGCTGGGGCC AATGCCACTA 120
TGTCACACAA CTCTAGGGGG CACCCCACAC ATTGTATTCT ATGTGAATGA TACCCCCGAC 180
CACAAAAATG AAAACCATGT GAATGGTGCC TCCTGGAGTT ATACACCTTG GTGGTTCAGG 240
CTGCGTTCTC TCCTAATGTC CACCTCTTAG AAAACAGATG GAAATCGTCC AGAAGGTCTG 300
TTACAGCCAG TTTTCTTTCA CCACCTGCCT GCAATAATTG TTAACATTTC TCCACATTTG 360
CTCTCTTTCT TGCTCTGCTT TACCATTTAA AAGTAAGATG CCCTTTGCAA AGTGTTTGTA 420
AGAAACACTT TGCCTCTAAA AACTTCAGCC TGAATCTCTA AGAGCAAGGG CATTCTCCTA 480
TGTAAAACAC AATGCCATGA GCACACCCAC AAAACTTAAC ATTGACAACA ATAATATTAT 540
CTAATGCACA CTCCACATTT GAGTGACCGC AATTGTCATC TGCGAAGCTT TAAAAATATA 600
CACATTCCCG ACCTCTCCTC TGGAAGTTCT GACTCAGTAG GGTGAGTCCC TGGATGCTGG 660
ATGCTTCAGT AGCCCCTAAA GTGATTCAAA TGTGCAGCCA GGTTTGACCC CACAGAAGAG 720
GGTTTCAGAA CTCTCAGGAA GACAAGAAGA CCTGGGTAGA GGCACCCCAA AAAGCACCAG 780
TCAGCTGAAG AAACAAGAGG ACATGCCTAT GGCCAAGCAG GTCGGTGCCA GGGTCTGAGC 840
TGCACCAGGC ACCAAACTCA GTCTCACAGC TGCCCACAGA TGGCTGAGGG CTAGCCGGGG 900
AGGAAATGGG GTCAGGACAG AGTGACACAA TGGTTCAGAG TCAAAGGATG GAAAGAAAGG 960
AGAGGGCACT CCCTCCAGTG GAGCTGGCTC TGTTTAGTCC CTGTGCCAGA GAGGGAGGAG 1020
CCCAGGGGCC ACCACTGGAG CCAGTGGGTG GTGAGGGTTC CTGCTGTCTT GCTGGAAGGC 1080
ACCCTAACAG AATTGTTCTC CTTGGGACTG GGAGAATCTA GAGGGGTCTG GGTCATCTCT 1140
TCCCCATACC CTGAGCCACA GATTGGATCC CAAAGGGTGT TGAGTACCAG CTACATGCCA 1200
GGCCAGGCAC ATACATATCT AAAGACTACA AGTATTCAGA TGACTATGGC ACAATTCCAG 1260
GGAGCTTACA ATCTAGCAAA GGTGGCAGAC ACATACATAA AGAATTCAAT CCCCTCTTGG 1320
GGTGTAAAGC AGGAAGCAAG AAGGTACTGC ATGTCTTGGA CCATCTTCAG TGGGCAGGGA 1380
AAATGGAAAG CTCTCAAGCA AGGCGGTGAA GAATATGCAG GGTTTCAAGC CCCCAGTCTT 1440
GGGCATCCTG ATTTTCAGTA GATTTTACTA AGGGAAGAGA CTCAGCTCTA GGACTTCCCC 1500
AGGAAGGGAC CCTCAGCACT TCCCCTAAGG ACAGGCAGGG TCAGGGAGTC AGAGGCCATT 1560
AGGACTTAAA CCCTTTGGTG TCCAGGTTTT TCTCTTCAGA GAGGACCTCC ACTTCTGTCC 1620
ATCCCCCAGC ACCCACACTC ACCCATACCC CCAATCCCAC CTCCTTTGCA GCCAGGGACC 1680
CTGCCTCGCA TCTCACTCCA CACACATGCC GCTGGCTCCA ACTGCCCCTC CCACAGCCCG 1740
GCTCTAACAG GGAACATCAA CACACTGCCA GGAATCCGAC TCCTACAGCA GGGAGGTGTA 1800
TTAAGGTCAA GCAAGCCGGC TCCCCCAGCC TCCAACAGAT GTGCATCTGA TCCCTGCTTC 1860
CTTATGGAAA ACCCACAGGT TGTATACAGC TCTATAAGCT TTTTTGATGG CAGGTCTATT 1920
ACAGAATCAC ATGCATCCAT AAGGTCTTTC TCTTCTCTAG TGTGCGTGCC CTCTGGGTGC 1980
CTCTCATCTA GTTCCAAATG TGAGAAGACA AAATAACAGC TTGTGTTTTC TTCCCACTTA 2040
TACATCCCCT CTCTAGTGAC CTCTATAGCT AAACTAAAGC AGCCGCACAT GGTCTGGCAT 2100
TTCCTACCAG GACTTACTCT CCATTATTCT ACTCTCTGGG CATACCATAC CCTGGACTCT 2160
CCATTAATTT GAAGCCAAAG TGCACACAAG AGTTTAGTGG AAGTCTTTCT GGGTCCTAGA 2220
CAATCAGAGG GACAGAAGCT TGGAGCCTGT GGGACACAGC TACATAAAGT CAGGTCTGCA 2280
TGCACTGCTG ACTCCAACTC AGAGACCCCG ATTCTAGCTC AGAAACCATT TGGTCTCATG 2340
CACACACATA GAATCCTTGG AGATCATAGC TCCTGCTACA TACCCTGTAG ACTGTGGGCT 2400
CTGTGTTATG AGGAGACCAG GATGGAAGAG GTGAGGCAGC TTGTGGCTCC TCTAAAAACT 2460
TTCCTTCCTC TAGAGCTGGC AATTTTGATT GCAGGGTCAG GAACCAGAAG CTGGCAATCA 2520
ACTGAATGGA ACATTTGGCA AAGAAGGAAG AAAAGCTTTG GCAGTACGTG TATTTCTAAC 2580
CCAGGAATCA TCCCAGGAGC CAGAGCAGCC ACATCTCTGT CTGGTTCCTA CTTCCTGCTT 2640
CCTCCTCCCC TCTTCCCTCA CCCAAGAACC AATCCTTCTC ATCCAGTTCA CCCCAGGTTC 2700
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