| Tag | Content |
|---|
EnhancerAtlas ID | HS017-01535 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr1:101652130-101654310 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:101652365-101652383 | CCTTCCTTCCTCTCTCTC | - | 6.25 | | EWSR1-FLI1 | MA0149.1 | chr1:101652333-101652351 | TTCTCCTTACTTCCTTCC | - | 6.41 | | EWSR1-FLI1 | MA0149.1 | chr1:101652361-101652379 | CTTTCCTTCCTTCCTCTC | - | 7.57 | | EWSR1-FLI1 | MA0149.1 | chr1:101652353-101652371 | CCTCCCTTCTTTCCTTCC | - | 7.82 | | EWSR1-FLI1 | MA0149.1 | chr1:101652345-101652363 | CCTTCCTTCCTCCCTTCT | - | 7.95 | | EWSR1-FLI1 | MA0149.1 | chr1:101652349-101652367 | CCTTCCTCCCTTCTTTCC | - | 8.37 | | EWSR1-FLI1 | MA0149.1 | chr1:101652341-101652359 | ACTTCCTTCCTTCCTCCC | - | 8.4 | | EWSR1-FLI1 | MA0149.1 | chr1:101652357-101652375 | CCTTCTTTCCTTCCTTCC | - | 9.09 | | EWSR1-FLI1 | MA0149.1 | chr1:101652337-101652355 | CCTTACTTCCTTCCTTCC | - | 9.25 | | Mecom | MA0029.1 | chr1:101652274-101652288 | TTTTATCTTTTCTT | - | 6.38 | | POU4F2 | MA0683.1 | chr1:101652881-101652897 | TTGAATAATAAATTAA | + | 6.5 | | ZNF263 | MA0528.1 | chr1:101652289-101652310 | CCTTCTTCTTTCTCTTTCTCC | - | 6.01 | | ZNF263 | MA0528.1 | chr1:101652292-101652313 | TCTTCTTTCTCTTTCTCCCCA | - | 6.02 | | ZNF263 | MA0528.1 | chr1:101652357-101652378 | CCTTCTTTCCTTCCTTCCTCT | - | 6.12 | | ZNF263 | MA0528.1 | chr1:101652302-101652323 | CTTTCTCCCCATCCCTCCCTC | - | 6.13 | | ZNF263 | MA0528.1 | chr1:101652349-101652370 | CCTTCCTCCCTTCTTTCCTTC | - | 6.32 | | ZNF263 | MA0528.1 | chr1:101652298-101652319 | TTCTCTTTCTCCCCATCCCTC | - | 6.39 | | ZNF263 | MA0528.1 | chr1:101652306-101652327 | CTCCCCATCCCTCCCTCCCTC | - | 6.63 | | ZNF263 | MA0528.1 | chr1:101652353-101652374 | CCTCCCTTCTTTCCTTCCTTC | - | 6.75 | | ZNF263 | MA0528.1 | chr1:101652310-101652331 | CCATCCCTCCCTCCCTCCTCT | - | 7 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I101187 | chr1 | 101652557 | 101653156 |
|
Enhancer Sequence | CTGTAAGTTT CCCGAGGTGT CCCCCAGCCA CATGGAACTG CAAGTCAATT ACACCTCTTT 60
TCTTAATAAA CTTCTCAGTA TCAAGCAGTT CTTTACAGCA ATGTGAGAAT GAACTAATAC 120
TTTCTTTCTT TCTTTCTTCT TTTCTTTTAT CTTTTCTTTC CTTCTTCTTT CTCTTTCTCC 180
CCATCCCTCC CTCCCTCCTC TTTTTCTCCT TACTTCCTTC CTTCCTCCCT TCTTTCCTTC 240
CTTCCTCTCT CTCTCTCTCT CTTTCTTTTT GGAAAAGGTC TTGCTCTGTA CCCAGGCTGG 300
AAATGCAGTG GTACAATCAT AGCTCACTGC AACCTCAAAC TCCTGGGCTC AAGAGATCCT 360
CCCATCTCAG CCCCCCGAGT AGCTGGGACT ACAGGCACAT GCCACTGCAT GCAGCATTTT 420
TTTTTTTTTT TTGTAGAGAT AGGCTCTTAC TATATTGCCA AGGCTGATCT CCAACTCCTG 480
GCCTCAAGTG ATCCTCCTGC CTTGGCCTCA CAAAGTGCTG GGATTACATG TATGAGCCAC 540
CACACCCAGC TCTATCTGAC TCTTTTCTTC ATACCACCCC CTGCAAAAGT CCTAAGACAA 600
ATTGTTGGCT CTTTTCATTC CACCACACCG TACAGATGGG CTACAGAAGA GCACCAGCAC 660
CCTTTCAGGG TTGTCCCCTA AGTCTACATG CCTAGCTCTT TAGTTCTCCC ATTGAATTCT 720
TTTTCATTGT ATCATATGAC ATATTATTAA TTTGAATAAT AAATTAAATT TTTATATTCC 780
TACTGCTAAG TCAGTACTGT GTATATAAAC TGAATTTCCC AGCTTTTCTT GGAACATGGT 840
GCTCACTAGA GGAATGGAAA TTCAATTTAA AACAATAAAT AGGGAAAGCA GAAAGAGTAA 900
ACAAAATGTG GAAGGGTGAG GCTTACTCTG AGGAGTGACT AAGCAGGCAG CTTCCTGTGG 960
GCCCTTTAAA AAATGATTTT TTAAAAAATG TTCTTCCCTA TTAGTTCTTA GAAAAGCAGA 1020
TCAACTTGAA AAGATGCTGG TAGTTAGGTA AAACACAGAT ATATGGGTTT TTTTTTTTTT 1080
TAAAAAAAAT GCAATAGAGA CTATGTTATT CTAATAGTCA TAATCTCTAA AACGGTTCAT 1140
CTATTTTTTT TTTTTTGAGC TGGAGTCTCA CTCTGTCCCC CAGGCTGGAG TGCAGTGGCG 1200
CAATCTTGGC TCACTGCAAC CTCCACCTCC TGGGTTCTAG CAATTCTCTT GTCTCAGCCT 1260
CCTGAGTAGC AGGGACTACA GGTGCCCACC ACCACTCCTG GCTAATTTTT GTGTTTTTAT 1320
TAGAGATGAG GTTTCACCAT ATTGGTCAGG CTGGTAAAAT GGGTCATCTT CTGCTACGTT 1380
TTAATAAGAA ACTGATACTC ATTCATATTC ATATAGATTC CTAATCTAGA AACTCAATCC 1440
ATAAACTGGA TCCTTTATGA ATTGCATAAA ATATAAATTA ATTTCTTTCA TTAAGTGTTA 1500
TGTAAATTTA TAATACAACA ACACCTGTTA CAATTTTTAA ATTTCTAATG GGCTTTAAAT 1560
ACTCAGCACC ACTGAGAAGC TTGCTATTGC CTTGTGTCTA TCAGTGTTTT CGCTCTAAGT 1620
TAAATGTACA TTCCACAACA ACAAACCACG TTTTGTTTTT TTTTTGGAGA TAGGCTGGAG 1680
TTCAGTGACA CTGAGCATAG TTCACTGCAG CCTCGACTTC AGGGCTCAAG TGATCCTCCT 1740
ACCTCAGCCT TCCAAGTAGC TGGGACCACA GGTGTGCACC ACCACACCCA GCTAATTTAT 1800
TTTTATTTTT GCTAGAGATG AGGTCTCACT CTGTTGCCCA GACTGGTCTT GAACTCCTGG 1860
CCCCAAGTGA TCCTTCTGAC TCAGCCTCCA AAATTGCTAG GATTACAGGC ATGAGCCACC 1920
ACAGCCAGCC ACAAACCACA TTTGTACTCT TCTCTTTTTA TTTACATTCC CCAAGTCAGT 1980
GCTAAGTACA GAACTGATGC TTAATAAATA CTTGATTGAT TGAGTTATGT GAATCTGTGA 2040
GAAGTCAATA GAAGTAGCCA TGAACTGTCA AACCTCAGAC TATATGATTA GAAATTCATG 2100
CTCCAAGGAA AGAGCATGAG GAGCTTGAAG TGAATCCTTG CTCAGGAATA TACGAGCGAT 2160
GTGACCATGA GGAAGTTACT 2180
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