| Tag | Content |
|---|
EnhancerAtlas ID | HS170-01937 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr19:16476740-16479330 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr19:16477854-16477865 | TTTTATGGCTC | - | 6.14 | | MEF2A | MA0052.3 | chr19:16477656-16477668 | TTTATTTTTAGC | - | 6.04 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_10209 | chr19:16475292-16484487 | CD19_Primary | | SE_11315 | chr19:16474290-16485342 | CD20 | | SE_11937 | chr19:16473771-16485687 | CD3 | | SE_14609 | chr19:16473598-16485678 | CD4_Memory_Primary_7pool | | SE_15445 | chr19:16475158-16485044 | CD4_Memory_Primary_8pool | | SE_15848 | chr19:16475046-16485222 | CD4_Naive_Primary_7pool | | SE_16360 | chr19:16475218-16485623 | CD4_Naive_Primary_8pool | | SE_17083 | chr19:16475450-16484473 | CD4p_CD225int_CD127p_Tmem | | SE_17319 | chr19:16468964-16489910 | CD4p_CD25-_CD45RAp_Naive | | SE_18015 | chr19:16473227-16488773 | CD4p_CD25-_CD45ROp_Memory | | SE_19662 | chr19:16473512-16478578 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20143 | chr19:16473448-16485693 | CD56 | | SE_20988 | chr19:16475387-16484302 | CD8_Memory_7pool | | SE_21494 | chr19:16475691-16485519 | CD8_Naive_7pool | | SE_21927 | chr19:16475508-16486069 | CD8_Naive_8pool | | SE_22683 | chr19:16473350-16485641 | CD8_primiary | | SE_31861 | chr19:16477431-16478097 | Gastric | | SE_50928 | chr19:16475528-16478306 | Sigmoid_Colon | | SE_50928 | chr19:16478724-16487174 | Sigmoid_Colon | | SE_53383 | chr19:16475646-16485667 | Spleen | | SE_55459 | chr19:16476277-16478310 | Thymus | | SE_55459 | chr19:16478837-16484301 | Thymus | | SE_61491 | chr19:16432573-16510994 | Toledo | | SE_62295 | chr19:16434424-16512260 | Tonsil | | SE_66507 | chr19:16476878-16478277 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 16477143 | 16477842 | | chr19 | 16477247 | 16477817 | | chr19 | 16478200 | 16479000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I016362 | chr19 | 16473350 | 16485630 |
|
Enhancer Sequence | GGTCTCCAGG GACCTGGGGC CCTTTGGAGC AACACCCTGG GGAGCGAGAA GGGAATAAAG 60
GCATCTGCCC TTCCTGGTTT GCAGGAAACA GCAATGTTAC TGTGCATGCT TGGGTATTTG 120
ATTTTTCCTC GAATACCTAT GTGATATGGA TCAAATAGCA AGATTCTAGC AGAGGAAACA 180
GTTAAGTGTT TCCAGGGGAG AAGCTCAAAG TCCCAGGACA CGGTGTAGCC CCCTGGGACG 240
GGCAGCAAGT CCAGGGTGGA CACTGCTTGA TTTCTCGAAG CCGTTCCTGC AGGGAGTGAT 300
CACCTGAGGC AGATTTGCAA GAATGTGGAG GGAGGTGTAA AGGGAGGACG CCCCAGCCAG 360
GCCCCCAAGA GCGACTGCCA CGGTACAGAA GGTTCAAATA AATCAGTCAT TTTTGAGCTG 420
CTTTTCTTCT TCTTTTCAAT GAAGATCTTC CTCCCTTGGT TTGGGGGGTT TAAAAAAAAG 480
AAATTGGTTT TTGGGAGGAG CGGTTAAGAA TTCTGCCTGC TACCATTTCA AGCTGAGGTT 540
TCTGATGCGC AAAGAGATGT TCAGAGAGAT GAAAAGCTTC GTTCACACCA AGAACTGCCT 600
GTGCCTGGTT TTGCTCTGTT GCCGAAACCG TTGTTATTTA GAAATCATGA CTATGGTAAT 660
ATGAAACCAG GGCACATCAA CTGCTGGCCT CTTGTTTTCA GAAGGAACAT CAACAACAAC 720
AACGGTTTTT TTCTCAGTTG TTAGTGTTTG TGCTTTGGTA AGAGAGGAGA TTTTGGACCT 780
GACACGTGTG AGGTCAGCCG AGTGCCCGGT CCAGCTCTCG ACCTTGCTAA TGACCAGACG 840
CTTTGAGCAA AGAAAGCCCC CGGCATCACT GTAGGGCCAC GGCCCTCAGC CCAAACTTCC 900
CACTTTTGCT CAGCGATTTA TTTTTAGCGG CTGTATTTTT CAAACCTTCT AGGTCTAGTT 960
CCTGCTTTTA TGTAACCACT TCTGCTAACT CCTTAATCGT TTTTTCCGAT TTTGTGAGGT 1020
ATAGCTTATC TCAAACGTGA CAAAGTAACT TTAATCTGCC TCCAGGCCCT GAAGCAAAAG 1080
CTGCCACGCG CACCCACGCC AGGGTTTTAT ACTTTTTTAT GGCTCCAGAA AACATGAGTA 1140
AGGAGAGAGC TTTACTGACG CGCATTTCAG AAAAGGGGAT GGAAATCATG AAAACAAAAC 1200
CCAAAAAAGT GGGTATAGAA ACATCTGGGA ATGATGGCAT CAAACCAGGT GCCAGGCATC 1260
ATCCTGGCAC CTGGTTCGAT GCCATCAATC CTAGATATTT GCAGCGGGAA CTACCGGGGA 1320
CCACAGCAGA CGGCAGTGAA TAAAGACAAA TGAAATTAAA GACCCTCTTG GGTGTGCTGA 1380
CTGCCTACCG CAGGGAGACT TCATTAACAG GGGGCAAGGG ATACAAGACT GAAGAAAACA 1440
CAAAATAGAA CTTATTTTCA AACCACAGCA GTTTCAACAG TTACCCAAGC GGTGTACCGA 1500
AACCACACAC AGGACTGACT TTAGCAAAAA CAATATGAAC CAAATGGTTT ACCACAGTAT 1560
GTGCTGTTAA AAAAAAAAAA AAAAAAAAAA AAAAAAACTT GGTGGCCGGC TCCACCCTGA 1620
TAGAAATTTC TTTAATTCTC CTATTTCTCA AGCTTCTTCT CGAGGCTGCG CACGCCCCTA 1680
GCACCCGGGA TCGGGGCTGT GATGGGGCTG GCTCTGCTGC ACTAGCGTTC TTGGTCAGCA 1740
AAGTTTTTCA AGGTTCTGAC TTTTCTATCT TGCTTTGCAG GAAGCCCTCC GCTTAAAAGC 1800
ATCCTCAAGA GCTGGGTGCA AAGCAAAAAA AAAAAAAAAA AAACCCAAAA AACAACAAAC 1860
AAACAAAAAA TTGAATAGAA ATATACAATT GCAAACCATA AAAACGGTGA ATGCTATAAA 1920
AACCTTGGAA AGGAAACTCT CTTGGTTTAA ATTTTTTGCT TAGGAGGAGC ATAAAAGGTT 1980
CAGGTGAGGT ATGGTCTCAA TCAATCCGAT TAATAAAAAT ATTAGTAATA AACATGAGAG 2040
TGAGAGAGAG AGAGAGTGTG TGTGTGTGTG TGTGTGTTTG ATCCTGGCTA GGTTCTGTTT 2100
ATACAGTTCA GTTCAGTGCT GTACTTGGAA AATGCAGTTC TGCAGATGAG AGATACATAC 2160
AAAAACAAAA AGAAAACAAA AAAATACAAA ACAAGGGTTT GTGGTCAGGG AAGCTGCCCA 2220
CCTTCGCTAT TATCCTATAC AACACAGAAC GATCACACAA CTCTCACTCA TCCTACACAA 2280
CTGTGGACAC ACATACACAA CCATCATTGA TCCTACACAA TGGGACACAC ACACACAAGC 2340
ATCACTGATC CTACACAACA GTGGACGCAC ACATACAACC ATCATTGATC CTACACAACA 2400
GGGGACACAC ATGCACAAGC ATCATTGATC CTACACAACA GGAGATGGCT ACACAACTGT 2460
CATTCATCCT GCACAATATG GACACTCACA CAACTCCCAT TCATCCTACA CAACAGAGGA 2520
TGCCCACACA ATTGTCATTC ATCCTGCAGA ACACAGACAC CCACACAACT GTCATTCACC 2580
CTACACAACA 2590
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