| Tag | Content |
|---|
EnhancerAtlas ID | HS127-01360 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr1:101652240-101654390 |
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 | GAACTAATAC TTTCTTTCTT TCTTTCTTCT TTTCTTTTAT CTTTTCTTTC CTTCTTCTTT 60
CTCTTTCTCC CCATCCCTCC CTCCCTCCTC TTTTTCTCCT TACTTCCTTC CTTCCTCCCT 120
TCTTTCCTTC CTTCCTCTCT CTCTCTCTCT CTTTCTTTTT GGAAAAGGTC TTGCTCTGTA 180
CCCAGGCTGG AAATGCAGTG GTACAATCAT AGCTCACTGC AACCTCAAAC TCCTGGGCTC 240
AAGAGATCCT CCCATCTCAG CCCCCCGAGT AGCTGGGACT ACAGGCACAT GCCACTGCAT 300
GCAGCATTTT TTTTTTTTTT TTGTAGAGAT AGGCTCTTAC TATATTGCCA AGGCTGATCT 360
CCAACTCCTG GCCTCAAGTG ATCCTCCTGC CTTGGCCTCA CAAAGTGCTG GGATTACATG 420
TATGAGCCAC CACACCCAGC TCTATCTGAC TCTTTTCTTC ATACCACCCC CTGCAAAAGT 480
CCTAAGACAA ATTGTTGGCT CTTTTCATTC CACCACACCG TACAGATGGG CTACAGAAGA 540
GCACCAGCAC CCTTTCAGGG TTGTCCCCTA AGTCTACATG CCTAGCTCTT TAGTTCTCCC 600
ATTGAATTCT TTTTCATTGT ATCATATGAC ATATTATTAA TTTGAATAAT AAATTAAATT 660
TTTATATTCC TACTGCTAAG TCAGTACTGT GTATATAAAC TGAATTTCCC AGCTTTTCTT 720
GGAACATGGT GCTCACTAGA GGAATGGAAA TTCAATTTAA AACAATAAAT AGGGAAAGCA 780
GAAAGAGTAA ACAAAATGTG GAAGGGTGAG GCTTACTCTG AGGAGTGACT AAGCAGGCAG 840
CTTCCTGTGG GCCCTTTAAA AAATGATTTT TTAAAAAATG TTCTTCCCTA TTAGTTCTTA 900
GAAAAGCAGA TCAACTTGAA AAGATGCTGG TAGTTAGGTA AAACACAGAT ATATGGGTTT 960
TTTTTTTTTT TAAAAAAAAT GCAATAGAGA CTATGTTATT CTAATAGTCA TAATCTCTAA 1020
AACGGTTCAT CTATTTTTTT TTTTTTGAGC TGGAGTCTCA CTCTGTCCCC CAGGCTGGAG 1080
TGCAGTGGCG CAATCTTGGC TCACTGCAAC CTCCACCTCC TGGGTTCTAG CAATTCTCTT 1140
GTCTCAGCCT CCTGAGTAGC AGGGACTACA GGTGCCCACC ACCACTCCTG GCTAATTTTT 1200
GTGTTTTTAT TAGAGATGAG GTTTCACCAT ATTGGTCAGG CTGGTAAAAT GGGTCATCTT 1260
CTGCTACGTT TTAATAAGAA ACTGATACTC ATTCATATTC ATATAGATTC CTAATCTAGA 1320
AACTCAATCC ATAAACTGGA TCCTTTATGA ATTGCATAAA ATATAAATTA ATTTCTTTCA 1380
TTAAGTGTTA TGTAAATTTA TAATACAACA ACACCTGTTA CAATTTTTAA ATTTCTAATG 1440
GGCTTTAAAT ACTCAGCACC ACTGAGAAGC TTGCTATTGC CTTGTGTCTA TCAGTGTTTT 1500
CGCTCTAAGT TAAATGTACA TTCCACAACA ACAAACCACG TTTTGTTTTT TTTTTGGAGA 1560
TAGGCTGGAG TTCAGTGACA CTGAGCATAG TTCACTGCAG CCTCGACTTC AGGGCTCAAG 1620
TGATCCTCCT ACCTCAGCCT TCCAAGTAGC TGGGACCACA GGTGTGCACC ACCACACCCA 1680
GCTAATTTAT TTTTATTTTT GCTAGAGATG AGGTCTCACT CTGTTGCCCA GACTGGTCTT 1740
GAACTCCTGG CCCCAAGTGA TCCTTCTGAC TCAGCCTCCA AAATTGCTAG GATTACAGGC 1800
ATGAGCCACC ACAGCCAGCC ACAAACCACA TTTGTACTCT TCTCTTTTTA TTTACATTCC 1860
CCAAGTCAGT GCTAAGTACA GAACTGATGC TTAATAAATA CTTGATTGAT TGAGTTATGT 1920
GAATCTGTGA GAAGTCAATA GAAGTAGCCA TGAACTGTCA AACCTCAGAC TATATGATTA 1980
GAAATTCATG CTCCAAGGAA AGAGCATGAG GAGCTTGAAG TGAATCCTTG CTCAGGAATA 2040
TACGAGCGAT GTGACCATGA GGAAGTTACT TAACTTCCCT GAGCTTCAAT CTTCTTAATA 2100
AAATGAGATA CCATCTCACA CCAGTTGGAA TGGTGATCAT CAAAAAGCCA 2150
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