| Tag | Content |
|---|
EnhancerAtlas ID | HS108-42419 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chrX:48995220-48997870 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chrX:48995297-48995308 | CATGAGTCACC | - | 6.62 | | HNF1A | MA0046.2 | chrX:48996181-48996196 | GGTTAATCTTTAACC | - | 6.26 | | HNF1B | MA0153.2 | chrX:48996182-48996195 | GTTAATCTTTAAC | - | 6.18 | | JUND | MA0491.1 | chrX:48995297-48995308 | CATGAGTCACC | - | 6.02 | | SPI1 | MA0080.4 | chrX:48996244-48996258 | TACTTCCTCCTTTT | - | 6.09 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTTGGTCAGG CTGCTCTTGA ACTCCTGACC TGAAGTGATC TGCCCACCTA AGCCTCCCAA 60
AGTACTAGGA CTATAGGCAT GAGTCACCAC GTGGGTCCCT GATGGAGAAA TTTTAATCTA 120
CACATCCAAG AAGTTCAATG AACAAGTAAG ATAAATGCAA AGAGGTCCAC ACCTAGTGTA 180
GGATCCCTGA GTTCCTCCTC CTTTCTTTTT GTGTTCTGAC CTAAAATCAC AGAGTGCTTT 240
GGCCATTCTT CCACCCAGCG AGCTGCAGGT TTTTCTCAGC AGGCTTGAAC CCAAACCAAG 300
GCCTTGAACA TTCCCAGGCA CTGATAAAGG TATCTGGGTT GTTGCCCAAG CACTGAAAGA 360
AACTGACCCT AGCCCTGAAC AAATTCCTTA AAGCCTCATA TAAACTCCAT ACCGTGACCC 420
TTTGGCTGTG GACATACCTA AGTAGAACAC CCCTTTTCTC TCATTGTCCC TCATAAGGAC 480
AGAGTGCTGT CTCTAGGAAT CGATGGAACT GGACTGGATC CCTGAGTAAA TATTTTAGTC 540
CAAGGGGAGG TCCACAAGCG ATCTGTCTCT GCAGCACTCT GTATGTAAAT TCCCCCAATA 600
TGCATTTTGG GCTTATCGCC CTGGCATTTA GTGCTTCTGT TTTTGGAATC CCAACTCATC 660
CCATCTCAGG ATCATTTTGT AGCAGGACGA GCCGCAGACA GAACCCCTCA GACACTGGGT 720
TAAAGAAGGA AGAGGCTTTA TTCGGCCAGG AGCATCGGCA GGCTTGCGTC TCAAGAACTG 780
AGTCCCAGAG AAAGAGTTCT TGGCCCTTTT AAGGGCTTAC AGCTCTAAGG GGTCCACATG 840
AAAGGGTCGT GATAGATTGA ACAAGCATGG GGTACATGGC TAGGTGGGGG TGGTGAGCAA 900
GGCAAGTGTT TCTCCATACC ATTGTCTGTG ATCTATAGAC AGCACAAGCG GTTAGGGTGT 960
GGGTTAATCT TTAACCTACG GGCCTGGCCA GTGGTGCTGA TCAGTCTGTT ATTTTTTCAG 1020
TTTTTACTTC CTCCTTTTCT TTGGAGATAG GGGACAGTAG GAGAAATGGC CTCTCTCCTC 1080
ATTCCCCCCT TTGAGAACCT CACTCACTAG TGGGAGTTCT CATTATCATC CTCACTATCT 1140
AGATCTTCCT GTGAGACAGA TCAATAGTGA TTCATGTAGT ATACTTGTGC TGAGGTCTTT 1200
TGATGAACTA AGGTGATAAC GAAGCTTCTT AGTAACTGGA GAAATATGGG TAACATACAG 1260
GGGAGTAACA TGCAGGTTCC TAACACCATT ATCATTCCTA TTATAAGAGT TTTAAATCCT 1320
CCTAGAGCTG GAAGCCATTT TCCAAACAGG GATCCAGGAT CAAACCTATG CCAAACCTGC 1380
ATGGGTACAT GTGCCAGCTT TGTCATGTCT CTAACTATAT TTTTGACTAC TTGTCCTTGA 1440
TCATCTCTTT GCAGACAGCA CTTGGTCAAG TTGAATTTTT CACAGACTCC TCCTTCAGCT 1500
GCCAGCAAAT AGTCTAAGGC CAATCTATTC TGATAGATGG CATTTCTCAT TTGGGTTTCC 1560
TGCTGGGCTA AAAGAGTTAA AGCTCTGCCA GTTTCACTAG TGATTATTTC TAAGATGGCC 1620
TGTAACCGTA TGATCCAGTT GAGCATGTAG ATGGGGGTAT GGTATCCCTA TGAGTCGTCT 1680
TGTGCCCATG TGGCAGGCCT ATAGTACTGT ATGATCCTTT CGGGGCACCA CTCATCATCT 1740
TTCCAATTTG CTATAGCTAT GCTCCTCTTT TCTTGGGAGG CATAGACAGG GAAACCTAGG 1800
AGGTCACCTG TTTTTATGGG CAGTAGGAAA AAGGATGGCT TAATGGTGCC AATGACACAA 1860
CTACCTGCCC ATTGATCAGG TAACTGAGTG TAGGCTCTGT GCCTACATAT CCAGTATAGT 1920
CCAGCGGGAG CCATCCAGTC TTGATGAGAT TGTGGATGGG CCTAAGCAGT CTGTAATTTA 1980
GGAAATTTAC TGAAGGGATT ATTTTCAGTA TGGTTTAGAC CCCACCAGGT GACTGTCCCT 2040
GTGTCCCTGT TATGCTTTTA TACAGCTTCT GTCCTAGACA ATTGAGCCTT CCTACAGGGA 2100
TGGTGAAGTC TTTTCCTTTT CTAGGTATGC AGTATTGTCC ATTAATAGAG GTTTTCAAGA 2160
CCCAAAAGTT GCTAGTTTGG GCCTTCTGGA CTGGAATTAT GTCAGGAACT GGATCAGTAG 2220
GCACTAATTC TTGGGTTTCC CAAGGCCATC AGTCTCCCAT AGTGGTTCCC TCACATACAT 2280
AACAGGAAGT AACATTGAGG GAATGAGCTA CATATTCTGC TAACTGGAGA AACAAGTTCT 2340
TTGTCCTTTT TTGTGGAAGC TCTGGTGCTG GCAGATTCAG CTCATCATAA AAGGTCTGAA 2400
ACACTGGTTT GGAAGATCGC TTGTGGACCT CCCCTTGGAC TAAAATATTT ACTCAGGGAT 2460
CCAGTCCAGT TCCATCGATT CCTAGAGTTA CATACTCTCC TGTTTTCCAG CAGGGATCAA 2520
GGGGATTGGT AATTAGTAGT TCAATGGGTT ACAGTGACCA CTAGTGCAGG AAGAGTTACT 2580
CTTTCCTTTT TGAAGGCGGA CAGGGTCCTT CTCATCTTTT TTTCCAGGTG GCCTAAATGA 2640
CACAGGACCA 2650
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