| Tag | Content |
|---|
EnhancerAtlas ID | HS091-00897 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:25614850-25617130 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:25616386-25616404 | CAAAGGAAGGAAGGAATC | + | 6.31 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGTAGAGATG GAGTCTCACT ATGTTGCCCA GGCTGGTCTC AAACTCCAGG CCTTAAGCAA 60
TCCTCCCACC TCAGCCTCCC AAAGTGCGAA GATTACAGGT GTGAGCCACC ATTCCTGGCC 120
TTAAAAGTGT GATATTTTTA ATGTATTTTG AAATCTGCAG GACTCTCCCT AGAAGATAAT 180
AGCAATAACC AACTCCTTTA TTGTGCTTGA CGTATATCAA CTCACTTTGC CCTTACCGTG 240
GCTCCAGAGG CATTGGGTCC ACCTTATAAA TGGAGGCACC AAGGCACAGA GTGATTAAAT 300
AAATTGCCCA GGATCACACA GCCAGAAAGT GTCTGAGTCA AGATTCCAGC CCAGGCAGCC 360
TAGACCTGAG AGCACGCTCC TAACCACTGC ACATCACTGT CTTAGCACCT CCTCAGCACA 420
AACTGGCCCT TGAGGAATGA AATACCGCCG CCGGCACACA CGCTCCTGAG TTAAGCCTTT 480
GTCAATGAAA TGAACACCCA CTTAAAAGGA ATAACCTGTC CAGGCACGAT GGAACATTGA 540
GTAACCCCTT ATTCTAAATT CCTGGTCCCT GTAAGACTCC TTCCCCATGC CCTTGCCCTT 600
TTCTGACCTT CCCCTAAAGT CCTTGAGGCT TAAGCGGGCA TAGTCTGCAG CAAACACTGG 660
GGAAGCTGAG TCCAGACTTC AGAGCACAGG CTTTGGATCT AGGCCAGCTG GATTTGAACC 720
TCACATTTGT GATCAGCTGG CATGACTGTT TCCAAAAAGT CCATTTTAAT CCTCTACGTG 780
ACCCTCTGTA AAATGGGATA CTGAATGGTG AGCTAGCACG ATTTTACAGA GAGTGAATTT 840
TTTTTGTGTG TGTGTGAGGC AGTCTTACTC TGTTGCCCAG GCTGGAGTGC AGTGGTGCAG 900
TCTCGGCCCA CTGAAACCTC TGCCTCCCGG GTTCAAGCGA CTGCCATGCC TCAGCCTCGA 960
GAGTGGCTGG GATTACAAGC ATGCACCACC ATGCCCGGGT AATTTTTGTA TTTTTAGTTG 1020
AGACAGAGTT TCACCATGTT GGCCAGGCCA CTCTTGAACC CCTGGCCTCA AGTGATCCAC 1080
CTGCCTTGGC CTCCCAAAGT GCTGGGAGTA CAGGCATGAG CCACTGCACC CAGCCTTATA 1140
GGGTTAAAAT TTAAAAGAGG TGATGCTGTT ACAAGCCTGT TTTACAAAAT GCTCTTATAA 1200
TAAATCATTA TCATCACTGT TGCTGTGGTT GTAGCATCAT CATCATTAAC TCCCAGAGGG 1260
AGGAGGGAGT CTCAGAGCAA GCTGCTCAGG GGAGACTGGA TGTCCATGGA TTGTCCAGCT 1320
CAGTACCACT TCCTCCAGGA AGTCCTCCCT GATAAGTCCA GTCAGCATCA CCCTCTCCTT 1380
CCAATGAACC CCACTAGCCT TGTGATATCA CAGATATTCT TAGTTGACAG GCTCATGGTG 1440
TAGCCTGTCT AGATCATAAG TACATTTTTT TTTTTTTTGG ATCATAAGTA TCTTCAAGAC 1500
CAAAATAATT TTCTACTCCT GAGCATGCTC ATTGGTCAAA GGAAGGAAGG AATCATAATA 1560
GCGTTAATAA GGCTAGCGTC TTTTCAGAAG TTGGTTCTTT GTGCCAGTCT TGGTGCTAGA 1620
CACACCGATA GGAAGAATAC TCCTTCACAT CCCCAGGACA CCAACATGGG ATACGTTTGA 1680
TCATCATTCT TAATTTGCAG AAGGAGAAAT AGGCTCAGTG AGATGAAATA GCCACTCCAG 1740
TGGCAAGGCT GGGACTGGAA GCCGGGCTTG TCCTGATTCC AAATCCAGTT TCTTTCCACT 1800
GCCACGGAGA CGGAGAGAAG GGACAGTGGC CCCAGATGGG GATGGGGTGA CTGGATGTGG 1860
GCAGGCCTGC GGGGGAAGAG TGCCCTCTGT TGAGCATCCG AATGATGGCA GCAGAAAAGA 1920
AGACTGGGCA GAATCCCAGT TATCAGATCC CCTGAGGGAA CAGTCACCCC GATCACCCTC 1980
AGTCAGATGA GTGTGTGTAG ATCAATGCCT CATAGATGAA GGCACTGAGG CACAGAGTGG 2040
TTAAGTCATC TGCCAGACCA CATGGCTCAG GGTGCAGAGG CCACCTTAAC GGGAGAAGAG 2100
ATGGTCACTC CACTCTGCAG CATCAGCGCC CAGGTGGGTA GAAATCTTGT CTTCTATTCC 2160
CACAGAAAGT AGGTGCCCAA CAGTGTTTGT TGAAAGAATG AATGAATGAA TGAATGAATG 2220
AATGAATGAG TGAGAGGCAT CCTTCCTTCT CAGTCGTCCT GGCTCTCCCT CTCTCCCCCA 2280
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