| Tag | Content |
|---|
EnhancerAtlas ID | HS052-10038 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr12:131316450-131318760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:131318588-131318606 | GAAAGGGAGGCAGGAAGG | + | 7.6 | | Klf1 | MA0493.1 | chr12:131317500-131317511 | AGCCACACCCA | + | 6.14 | | Nr5a2 | MA0505.1 | chr12:131316602-131316617 | GCTGGCCTTGAACTT | - | 8.42 | | OLIG2 | MA0678.1 | chr12:131316786-131316796 | ACCATATGGT | + | 6.02 | | OLIG2 | MA0678.1 | chr12:131316786-131316796 | ACCATATGGT | - | 6.02 | | Zfx | MA0146.2 | chr12:131318688-131318702 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 131316455 | 131316673 | | chr12 | 131317295 | 131317765 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I130830 | chr12 | 131314863 | 131318444 |
|
Enhancer Sequence | TGTCACCCAG GCTGGAGTGC AGTAGCGTGA TCACAGTTCA CAACAGCTTC AACCTCCTGG 60
GCTCAGGTGA TCCCTTTGCC TCAGCCTCCT GAGTAACTGG GACTACAGGC ACACATATTT 120
TTTTAGAGAT GAGGTCTGGC CATGTGGCCC AGGCTGGCCT TGAACTTCTT GGCCCAACCA 180
ATCCTCCCAC CTTGGTCTCC CCACGTGCTG GTATTACAGG CATGAGCGAC TACACCCGGC 240
CTGCCTCTGC AATTTAATCA TTTTTTTTTT TCCTCTCAGC TATACATTCA TATTTCTCCA 300
CTCAGCATAT ATTGCTCTAG TGTTAGGTGA AACCACACCA TATGGTTCAA CCTCATACAT 360
TCATCTTACT GCTGCATACA CTCCATTATA TAAACAGCCA TGAGGTAGCC ATCCAGGCTC 420
CTATTGTGCC TAATATTTTT CCATTACCAA CAATATAACG AACCACAGTT ACAAGGCTGC 480
ACATGCATGT CAGGATGGTT TTCTGGAACA TACACACACA TGCAGAGAGA GGACCACCGA 540
GCCATGGGGT TTAAGCGTCT TCAGCTTCAC TAAACAATGC CAAATTGCTC TCCAAAGCAC 600
TTGCAATAAA TTGGATGCCC CCAGCATGGC ACATGGACAT GAGACACTGC CAGGCTAATC 660
TTGAGCTACC AAGGGCCCAC CACATGATCT CGCCCCAGGA ATGAGGATCA GAACTGACAT 720
GATGAAGCCT AGAGAGCGTG AACTAGAGAG CATTTAAACT TGGGGGCGGG GGCAGCCCCT 780
TACACCAGGC CGTGGAGACG AAGAGAAACC CTCAGGATCT CGCTCCAGCC AACCTCCTCA 840
GCTCACTCAC GTCTCACCTC CGCCCACTGC TGACCATCCA CTCACTACCG ACAGCATCTT 900
TCTGTCCCTT GCATGACTTC GTTCCCAACT CTGGGCCTCT GGACTTGCTG TGCCTTCTAC 960
CCAGGGCACC CTCCCCCAGC CCTGTCCACA GCCGCTTTCT TATCCACAGC TCAGCTCACG 1020
GGGTGGCCCC CTGACCCACC CGGCCAAGGC AGCCACACCC ACACCCTCGC CCTGCTTATT 1080
CCTTCACAGC AAGGATTGCG AAAGACACTT GATTCATCTG CTCAGCTGCT GTCTATCTCC 1140
CAGCTGCAGG TTCCACAAGA GCAAGGACTT CTGTCTTTTC ACAACCCAGG CATTCTGCCC 1200
ACAGCAGTGC CTGGCACCCA GCCGCCAGTC AGTGATGACC AGGTCAACAA ACGAGTGAAT 1260
GAATGAATGA AGAGCAAGAG AAGGGCAGAC ACAGACAAGG GGGAGGAGAG TGGGAAAGTA 1320
CACACAAATG ACAAACGTCA ACAAACGGAA ACAGAGACAC ACACACAGAC TAAGACCCCG 1380
CAAGCACAAA ACGGCCACGA CACAAGGACA GGAAGGACCT CAGTGGCTCG CTCCGTCCTA 1440
ACTCCATCCC TCATGAGGGC TGATGGTACT ACGTGCCCTC AAAGCCTGGG AGAAATCACT 1500
CTACCTTTTT TTTTTTTTTT TTTGAGATGG ATTCCCACTC TGTTAGCCAG GCTAGAGTGC 1560
AGTGGCAGGA TCTTGGCTTA CTGCAACCTC CACTTCCCAG GTTCCAGCTA TTCTCTCACC 1620
TCAGCTTCCC AAATAGCAGA GATTACAGGC ACCTACCACC ACCCCCAATT AATTTTTGCA 1680
TCTTTAGTAG AGACGAGGTT TCCCCCTGTT GGCCAGGCTG ATCTAGAACT CCTGACCTCA 1740
AGTGATCCTT CCACCTTGGA CTCCCAAAGT AGTGGGATTA CAGGCGTGAG CCACCCCACC 1800
CAGCCCATTC TGCCTTTTAA TAAATCTCCC TTTTCTGCTT TAGCTGATGG GTTTCTGTCC 1860
CTTTTAACCA AAAGGCCTTG AAGACAACAG ATTCCAGTGG CATCTACATT TTTCTTACCA 1920
TGGGCATTTT CAAATGGAAA CAGACTGATT CAATAAATAC CTGGCAGGTG CTCTGGATCA 1980
GGCACCATGC AGAATACTGA GGCTTCAGAG CACAAATGAC AGTATGCATC TGTCCTGAAA 2040
AGGCTGAAGC ACTGGGGGAA GGGTGCAGGA AAAAACAGGA CTGCATCTGT GTCCAGAATG 2100
CCCCAAGACA AGATGGGCCA TCTGTGGGAA CATGCGAGGA AAGGGAGGCA GGAAGGCTTC 2160
CCAGTGATGC CTAACCTGAG ACTAAAAAAG GTGCAAGGCT ACATGTGGTG GCTCACGCCT 2220
GTAATCCCAG CACTTTGGGA GGCCGAGGCG GGTGGATCAC CTGAGGTCGG GAGTTCGAGA 2280
CCAGCCTGGC CAATGTGGTG AAACTCCACT 2310
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