| Tag | Content |
|---|
EnhancerAtlas ID | HS092-04322 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:201906410-201909060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:201908199-201908217 | CCTGCCTCCCTGCTTTCC | - | 6.07 | | EWSR1-FLI1 | MA0149.1 | chr1:201908211-201908229 | CTTTCCTTCCTCCCCTTC | - | 6.42 | | EWSR1-FLI1 | MA0149.1 | chr1:201908203-201908221 | CCTCCCTGCTTTCCTTCC | - | 6.93 | | EWSR1-FLI1 | MA0149.1 | chr1:201908207-201908225 | CCTGCTTTCCTTCCTCCC | - | 6.94 | | Foxd3 | MA0041.1 | chr1:201906574-201906586 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:201906895-201906907 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:201906899-201906911 | AAACAAACAAAC | - | 6.32 | | Foxo1 | MA0480.1 | chr1:201907912-201907923 | TGTAAACAGCA | - | 6.14 | | HES2 | MA0616.2 | chr1:201907399-201907409 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr1:201907399-201907409 | GGCACGTGCC | - | 6.02 | | ZNF263 | MA0528.1 | chr1:201908212-201908233 | TTTCCTTCCTCCCCTTCCCCT | - | 6.01 | | ZNF263 | MA0528.1 | chr1:201908211-201908232 | CTTTCCTTCCTCCCCTTCCCC | - | 6.12 | | ZNF263 | MA0528.1 | chr1:201908203-201908224 | CCTCCCTGCTTTCCTTCCTCC | - | 6.71 | | Zfx | MA0146.2 | chr1:201907500-201907514 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_01564 | chr1:201907442-201909415 | Aorta | | SE_26882 | chr1:201907436-201909403 | Esophagus | | SE_38927 | chr1:201907366-201909413 | IMR90 | | SE_48164 | chr1:201907418-201909844 | Psoas_Muscle | | SE_50558 | chr1:201907355-201909409 | Sigmoid_Colon | | SE_53198 | chr1:201907461-201908331 | Small_Intestine | | SE_53198 | chr1:201908462-201909393 | Small_Intestine | | SE_54511 | chr1:201906859-201909726 | Stomach_Smooth_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I201937 | chr1 | 201906508 | 201908122 | | GH01I201939 | chr1 | 201908636 | 201909149 |
|
Enhancer Sequence | CAAATAATTT AAAAATTATC TGGGCGCGGT GGGACACACC TGTAGTCCTA ACTACTTGGG 60
AGGCTGAGGC AGGAGGATCC CTTGAGCTCA GGAGTTTGAA GCTGCAATGA ACTGAGATTG 120
CACTACTCTA CTCCAGCCTG GGCAACAGAG TAAGATCCTG TCTCAAACAA ACAAACAAAA 180
AAAAACAAAA ACAAAAAAAC AAAAAACACA GTGGCTCATG CCCGTAATCT CAGCACTTTG 240
GGAGATTGAG GTGGGCAGAT CATTTGAGCC CAGGAGTTCG ACACCAGCCT GGGCAACATG 300
GTGAAACCCC ATCTCTACTA AAAATACAAA AAAATTAGCT GGGCATGGTG GTGCACAACT 360
GTAGTCCCAG CTACTCTGGG GGCTGAGGCG GGAGGATTGC TTGAGCCCAT GAGATGGAAG 420
TTGCAGTGAG CCAAGATCAT GCTACTGCAC TCCATCCTGG GGAACAGAGT GAGATCCTGT 480
CTCAAAAACA AACAAACAAA CATAGACTGT AACCTCTATG AGGGCAAGAA CCTTGTCTCT 540
CTTGTTCACT ACTCTATCCT GGCATTTAGA AAGTACATAA TAGGAACTCA TTAAAGAGCT 600
GGCAAATTAA TGATTTAATG GAGTCCTCCT CCCTCCTTGT AAACATAAAG CATGATTCAT 660
GAATTCTGTG TATAAAACGA ATGAAGAGAA TGGGAATGGG AGGAGCGGAT AGGAGTGAAG 720
GGAAGGGAGG AAACTAATGT TCATGGGCCT TTACTACTAG GTTTCCAACC CAGCACTCTG 780
CTTAGTGCTT TATGTGGATT ATTTTGCTGA AACCTCATAA CTATCCTATG ACTAAGCATT 840
GTAATTTCCT TTTTTTTTTT TTTTGAGATG GAGTTTCGCT CTTGTTGCCG AGGCTGGAGT 900
GCAATGGCAC CATCTCAGCT CACCACAACC TCTGCCTCCT GGGTTCAGGC AATTCTCCTG 960
CCTCAGCCTC CCGAGTAGCT GGGATTACAG GCACGTGCCA CCACGCCCGG CTAATTTTGT 1020
ATTTTTAGTA GAGACGGGGT TTCTCTATGG TAGTCAGGCT GGTCTCAAAC TCCCCACCTC 1080
AGGTGATCTG CCCGCCTCGG CCTCCCAAAG TGCTGGGATT ACAGGCATGA GACACCGCGC 1140
CCGGCCGTAA TTTCCATTTT ATAGGTGAGG AAACTCAGGC TCCAAGACGT GAAGTCACTT 1200
GTTTGGGTCA TTCAGCCAGC AACCAGCAGA GCTGGATCTG CACCCAGGTC TAGCTGGCCC 1260
CTGAGGAGAC TATTCTAACC ACTAGACTCA TATAGTCTGC ACTCAGAGCT TCCCTGGGAA 1320
TTTCTGCCTG AGGATGTAGC ACCTTTCACC TGCCAGTCTC AGGGACAGGG GTCCTGCCAG 1380
CCCTGCCGGC TTGATCTCAA AGGAAGGCCT ATTGAAGTAA CAATCAGAAG GAGCCTGTGG 1440
GCTGTCCATG AAAGGGTGGT GGAAGGGTGT GGGAACAGGA GGTGCTTCTA TTCCTAGCTG 1500
TTTGTAAACA GCATCCCGAC AACCCGGCTT GTTCTTTCTG CAGTGGGCCC CAGGGACAGC 1560
TGAAGCCAAG TTCTCCCAAA GCAGCCTTGG CTTTTCTGAG CTTGTGCTGG GGTGGAAGCC 1620
TGCAGACAAG GAGAATCCAC CTCAAAATCT TCTCCTAATC TCCTTTCACT CTGTCTTTTT 1680
CCAACCCAGC AACTCAGTTT GGGCCCCTGA GCCTGTGACA TAAAATAAAT TAGGCAGAGG 1740
CTCAAAGAAA TCAGGCTGCT GGGGCCAGGC AGCGAGTAAT TACATAAGCC CTGCCTCCCT 1800
GCTTTCCTTC CTCCCCTTCC CCTCTCTCTT CATCATTCCT TCACACTCAC TGATGGTTTT 1860
TTTTTTTTTT AATTTCGTGA GAGATAAAAT AATGTTGATT TGGCAGATAT ACAGGTACAA 1920
ACTCTGAAGA GTTTAGAGTG AGGAAAGAAG GTCTCTCGTG ATGTGCCAAA CACTTTCAAT 1980
GCCTCATCCT ATTTAATCTT CACTATAACC CTTCAAGGAT GATTTTATCA TCCCCACTTG 2040
ACAGGTGAAG TAATTGGGCC TCAAGAAGCT ATGTTAATGA GATAGCATCG ATAAAGCCTT 2100
TGGCTCCAGA AGGCACTCAA TCAAGTTAAT GTTCTTTCTT CCTTGGGTAA CTTATTCCAA 2160
GTCACTGGAT CAGTAAGGGG CAGGAGCAGA ATTCAAACCT GGACCTATCT GATTCCAGAC 2220
ACCCCTGGGC TTTCTGTCTC ACCGCACTGC CCAGACACTA ACAAGCCATT GGGAGAACTG 2280
ATGAACCGAA TGGAGACCAC TGCTCTTTTG CTGGTTAAAC AAAAGTGGTC CAATAAATAA 2340
GGAAGGGCCT GATCTGGAAA GGCCTGCATT CTATGGCTCA GGATATTCCT GTTTATCCAA 2400
CTTGGCAGGC ATGTAAATAT TAGCGTCGCC ACTCCTGTCC CCCATGCATG GCGCTGTGTG 2460
TTGTTCCTCT GCTCCTGCTG TGTGTGTGTG TGTGTGTGTG TGTGTATACA CATGTGTGTA 2520
GACTGCCTAT CTCTTGGTGT GCTTCATTCA GGCTCTGCAC ACTCTGGGCC CAGCTGTAGA 2580
TATGCTGACA CGGTCTGACA AAGATACTCT AAAGTCTCCT GGGGGAGAGA AAGAGAGACT 2640
GAAGGAGGAT 2650
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