| Tag | Content |
|---|
EnhancerAtlas ID | HS019-05584 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr15:65183490-65186270 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr15:65185134-65185151 | GGGAACACAGCGTGCCT | + | 6.14 | | Ar | MA0007.3 | chr15:65185134-65185151 | GGGAACACAGCGTGCCT | - | 6.18 | | NR2C2 | MA0504.1 | chr15:65185196-65185211 | TGCCCTCTGACCTGC | - | 6.56 | | ZNF263 | MA0528.1 | chr15:65184082-65184103 | TCCTTCCCTGTCCCCTCCCCC | - | 6.09 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_00179 | chr15:65184020-65192302 | Adipose_Nuclei | | SE_00949 | chr15:65185012-65191657 | Adrenal_Gland | | SE_04179 | chr15:65184024-65186890 | Brain_Anterior_Caudate | | SE_06037 | chr15:65183266-65190782 | Brain_Hippocampus_Middle | | SE_07417 | chr15:65183823-65188537 | Brain_Hippocampus_Middle_150 | | SE_09222 | chr15:65182907-65191234 | CD14 | | SE_12439 | chr15:65183446-65188936 | CD3 | | SE_13731 | chr15:65184779-65190340 | CD34_Primary_RO01536 | | SE_19509 | chr15:65183157-65189177 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20451 | chr15:65183543-65189374 | CD56 | | SE_25922 | chr15:65183499-65191039 | Duodenum_Smooth_Muscle | | SE_26878 | chr15:65183325-65190494 | Esophagus | | SE_29936 | chr15:65183762-65184608 | Fetal_Muscle | | SE_29936 | chr15:65184729-65188809 | Fetal_Muscle | | SE_31256 | chr15:65183577-65189571 | Fetal_Thymus | | SE_31840 | chr15:65183571-65184653 | Gastric | | SE_31840 | chr15:65184688-65191003 | Gastric | | SE_42313 | chr15:65183256-65191830 | Lung | | SE_43954 | chr15:65183041-65189653 | MM1S | | SE_50230 | chr15:65183230-65191055 | Sigmoid_Colon | | SE_52555 | chr15:65183178-65191028 | Small_Intestine | | SE_53569 | chr15:65182985-65192126 | Spleen | | SE_55484 | chr15:65183811-65189118 | Thymus | | SE_59387 | chr15:65156174-65198203 | Ly3 | | SE_62974 | chr15:65169474-65198305 | Tonsil | | SE_67436 | chr15:65183041-65189653 | MM1S |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr15 | 65183539 | 65183834 | | chr15 | 65183886 | 65184072 | | chr15 | 65184085 | 65185493 | | chr15 | 65185114 | 65185342 | | chr15 | 65183983 | 65184442 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I064891 | chr15 | 65183201 | 65190998 |
|
Enhancer Sequence | TTCCTAACCA CAGGGAGCTA TTGCATTTCA GGGTATCTTA CTCTAAAGGC ATGCTGGGAG 60
GAGGTGAGCA CTCCTTTGCT ACCTGTCCTG GAGTTGACCA AGCCCAGGGG GAAGTGCCTC 120
CTGGTGTCCA GCCTAAGTCC CCTTGCTGCA AAGTCAGTTC CTGCTCTTGT GTTCTGTTCT 180
CAGTGGATGT GGGAATTAGT TAGAGACCCT CCTCAGAGGG GCAGCCTGAT GATATGGAAA 240
GGCTTATAGG ACGCTGGGTT CAATCCTGGC ACTCCCACTG TCTTGCTGTA TGCCCTTGAG 300
TGGGTACTCA ATGCCTCTCT CTAGGTGTGG GTTTGCTCAT CTGTAAAATG AGGAGGCCAG 360
TTTTGACTGT GAACCCAGCC CTCTTCCCCA CTTCCCCTCT CCCATTGCAG ATGGGATGGG 420
TAGAAGGGGC AGGGGCTCCT GCCTTTTCCT ACTGAGCAAC TAATTTGTGT TTCTCCTCTG 480
GTCAAGGATG TGGGAACTGG GAGGGAGCAG GGCAGTGTGG GATGGTGGAG GAGAAGAAGT 540
TGCTGATGAG AGTGGGAGGC TGGCTGCCAC TAAGCCCTTC CCTACTGGAA ACTCCTTCCC 600
TGTCCCCTCC CCCAGACAAC CTCAGGAAAG GGTCTAGGTG TTTCCACAGT GGTCTAGGAA 660
GGGCTAGACC AATGTGGAGT GGACGACATG CCTGGTGTCT CCCTCTGGAG AGTGCACTCT 720
GGATACTAAT CTGAGTCTCC AAAAAGGAGA AAGGGTTAGG GATCATTTGG TCTCACCTTC 780
CCTCCTGCTT TTACAGAAAG GGAACCAGAG AGGTATAGTG ACTTGTTTAT GTCATGCAGT 840
GACTTGACAG CACAGTGGGA CATGAACTTG GAGTCTTGGA TGTGCAGTCC TGATCTTGCT 900
CCCAGCACTG CTCAGGGAAG ACATTCTTCC TGCTCTGCCT TCCCACCTCT CCTCCCAGGC 960
TCCTGTGATC CCCACAGGGA GAGCTAGAGC TTCTATAAAA ACTGCTGTAA TTGATTCTTA 1020
ACAGGAAGTG AGGGCTTTTT CACTTTGAGT TGACAACCAC AGCAGCTACA CACACACACA 1080
CACACACACA CACACACACA CACACAAACA CACACACAAA CACAGACATA CAGTTAAGGT 1140
TTAAATATCT GTCCCCTCTG AAACTCATGT TGAAACTTAT TCCCCAATGT GGCAGTAGTG 1200
AAAAGTGGGA TCTTCAAGAG GTGATTGGGC CATGAGGACT CTGCCCTCAT GAATAGATTA 1260
ATTCATTCAT GGATTAATGG ATTAATGGGT TCATGGATTA ATGGGTTATC ACGGGAATTG 1320
GACTGTTGGC TTTATAATAA GAGGAAGAGA GATCTGAGCT AACATGCTCA ACCCCATCAC 1380
CATGTGATGC CCTTCAGGGC CTCAGGACTC CGCAGAGTCC CCACCACCAA GAAGGACCTC 1440
ACAAGGTGCA GCCCTTCAAC CTTGGACTTC TCATTCTCCA GCACTGCAAG AAAGAATTCC 1500
TTTTCTTTAT AAATTACCCA GTTTCAGGTA CTCTGTTACA AATAACAGAA AACCGACTAA 1560
GACACACACA CCCCAAGTTT GTACACAACC ATGTGCACAC ACACAGTCAC TTGCCCATAC 1620
TCCTACGCAT TCAGGCACCC AGCTGGGAAC ACAGCGTGCC TTTCTTTCTA GTGCCACAAG 1680
ATACCCATTT ATAGGCTTCC AGCTTGTGCC CTCTGACCTG CCTTACATTT TGATAGTAGA 1740
GGGTGGATTT GAGGGGGAAG AGCAGAGACC ACAAGACCAG GCAGGGTTTC CTCAGTGGCT 1800
GCACTGCAGG GATTCAATGG GCAGCAAAGG CCCCCACACC CCAGGCTGGG CCTCATGGCT 1860
GAGACTCATC AGTCTTGGGC CTGGAGGGGC TGCTCTCAGT CTAACAGGCC TGACTGACAG 1920
GGAAACCACC AATTTGTCAT TGGGTTCCAA TCCCGAGTAG CTGGGATTAC AGGCGTGCGC 1980
CATGACGCCT GGCTAATTTG TTTTGTATTT TTAGTACAGA TGGGGTTTCA CCATATTCGC 2040
CAGGCTGGTC TCAAACTCCT GACCTCAGGT GATCTGCCCG CCTTGGTCTC CCAAAGTCCT 2100
GGGATTACAG CCGTTAGCCA CCTCACCCGG CCAGACAAAT GTTTGTTGCA TGAATGTCTT 2160
GCCCCTCACA TCTGTGTTCC GTCCAGCCTT CCTCGCCTCT CCTTTTTCTT GGTGCCCTGG 2220
CTGTGGCCAC AGTACTTTCC TAGGAGGAGG CCTATGCAGG CGCGTAAGGA ACTCGGTGAA 2280
GGAGTCAGGG CCCCCAACTC GGCTCTCGCG AGCTTGCTGT GTGACCTCAG GCCAGTCACC 2340
TCCCCTCTTC TGGCCTGGGT TTCCACACCT GCACAATGGG AACAGCAACC TCAGCTGCCT 2400
GCCGTCTCTG ACGTGAGGGC CAAATAAGAA AAGGTGAGAA GCTGGTCGCA AAGCGGTAAA 2460
AAAAGCCTTC AGCGCCGAAG CCGGGGAGGA AGCCGCTGAT GAAGCTATTG CTGAGAAGTG 2520
TGAAGCCCCC ACCCGAGGAT CCGCTTTTGA AGAGGGACCC GGGGAACGCG TAGGGGGAAA 2580
CTGCCTTCCT CTTCCCTCAG TGGAAAGGGC TGTGCTCATG TCACTGTGAA ACGAAGCTAT 2640
TTTTATGTAG TACAACTGCG ATTATGACAG GGCCTCTTCC TGAAGGGGAA GGGTGGGGAG 2700
GAGACCTGAG TCATCAGTGG GGCGGCCGGC CCCACAGGCT GACACAGGCA GCTTGTGGAA 2760
ACCAGGCCCC CCGCCCTGCC 2780
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