| Tag | Content |
|---|
EnhancerAtlas ID | HS091-44148 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr7:75648580-75650930 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr7:75650642-75650656 | CCCGCCTCGGCCTC | + | 6.01 |
| | | 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 |
| GH07I076020 | chr7 | 75649521 | 75649710 |
| Enhancer Sequence | GAACTCTAAC TGTTTTTTTC TTTTTTTTTT TTTTTTAAAT ACGTTTTTTT TAGAGACAGG 60
GTCTTACGCT GTCAGCCAGG CTAGAATACA GTGGTACAGT CATAGCTCAC TGCAGCCTTG 120
ACCACCTGGG CTCAAGTGAT CCTCCTGCCT CAGCCTCCTG AGTAGCTGGT GCTACAGGCA 180
TGCACCACCA TGCCTGGCTA AATTTTTTTT TTTGTATTTT TGGTAGAGAC GGGGCCTTGC 240
TATGTTGCCC AGGGTGGTCT CAAACTCCTG GCTTCAAGCA ACCCTCCTGC CTCAGCCTCA 300
CAAAGTGCTG GGATTACGAG TGTGAGGCAC CGTGCCTGGC TAACTCTGCT TCCATATTGA 360
ATTTTTGTTC AGGGAGACAA AGACACTTCC AGAAGGGGCT GTGGAGGATA TAAGTGGCTG 420
GGACCTATCT GAGAGATGGC ATTGACAGGA AGAATCTGGA ATCTGCAGCC AGGCTGAGAG 480
AGAATCTGCA GCTCTCAAGA CAGGAGCCAA AGCTCACCCC ACAGGGCCTG GCTCAGAAGT 540
CAGAGTTCAG GCCAGGCATG GTGGCTCATG CCTGTAATCC ATGCACTTTG AGAGGCCAAT 600
GCAAGAGAAT TGCTTGAAGC CAAGAGTTCG AGACCAGCCT GGGCAACAAA GCGAGACCCT 660
GACTCAAAAA AAAAAAAAAA AAAAGAAAGA AGGGGGTGTT GAGAGAAGCC TTGAGATGGT 720
CTTGTACCCC CAAAGACTTT TCATTGACCT GAAAGATGCC ATTTGAAACA AGAAAAGTTG 780
CCTTGAATGC ACAAGTTGTG TGGTTGTGGT TTCCTGTGAA TGGGGGCCCC ATAGCAAAGT 840
AAGGTCAGTT ATAGAATGTA AAGGGGATTA TCCATGTTGA GTACCATCTC CTAGGGTTTC 900
AAGGCCTAGC CTACAGTCCT AGGATTGCAG ACCAGAGCCC AACAGGATGA GCTTAGGGAA 960
GAAGGGACAA TTTCCTGGCC AAGGACCTCC TGGGACAAAA GTCCAGACAG CTGGTTTTAT 1020
GAAAGGTGGG AGCATAGCGC CACCCCGTGG CAGTTGGTGT GAGTGCCCCC AGCTTCTGGA 1080
ACGGCACCCA CAGGTGCAGT TCTGATTCCT AGAAGCAGAG CTCCCAGTGC CAATGGCAAA 1140
GGGTGGTCAG CCCAAAACCA GGGGCTAATG AAGAACACAG CAGAGCCTCA GAGGTTCGAT 1200
GGAGCACATT GGAACTGACC ACGCTTTAAT GTTCTGACTT GGGGCTGCAT GCTCTCGTGC 1260
CACTACCCAA TCCCTGGGGG ACAGGACAGA GCCAAAAAGG CCTGGGTTTG AATCCTGGCC 1320
CCACCACTTA TAGGTGTGGT GGTTTAAAAA TATGTCCACA ACACTTTTAA AAGCTTAAGT 1380
CTCAGGCAAC ACAGCAAGAC CCAGTCTTTA CAAAAAGTAA ATAAATGAGC TGGGTACCTT 1440
ATCTTGCCAT ATCACCCAGG CTGGTCTTGA ACTCCTGGGC TCAAGTGATC CTCCTGCCTC 1500
AGCCTCCCCA AGTGCTGGGA CTACAGGTAT GAGTCACTGG GCCTGGCTTC CTCACAGCTC 1560
TTGATGTTAG TTAGCGTCCT TGTAAGCTGT TCTGCAGATC CAAGTAAAGC CCTTGGTTCC 1620
TGGTGCATGG CACACATGGA ACTGTCCCCA TAAACTTTGT GAAATCAGCA AAGAAGGGAG 1680
GGGAACAAAT GAAAATAAAG CAAGCTTGCA GCACATTCAG CATTCATCAC TAAGTCACCT 1740
TGCTTGCTCT CCAACCTGCT TGCTCACAGC TGTTTGATGT GTATTGTCCT AGAATCACAT 1800
AAGACCCTGT TACAAGAATT TTTTTTTTTT TTTGAGAAGG AGTCTCGCTC TGTCGCCCAG 1860
GCTGGAGTGC AGTGGCGTGA TCTCCGCTCA CTGCAAGCTC TGCCTCCTGG GTTCACGCCA 1920
TTCTCCTGCC TCAGCCTCCC AAGTAGCTAG CAGGGACTAC AGGCGCCTGC CACCATGCCC 1980
GGCTAATTTT TTGTGTATTT AGTAGAGACG GAGTTTCACC GTGTTAGCCA AGATGGTCTC 2040
AATCTCCTGA CCTTGTGATC CGCCCGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCAT 2100
GAGCCACCGC GCCCGGCCAA GAATATAGTT CCCCTTAACT GCTCTGTAGG TGACAACTTG 2160
AACATCATGG AACACTGTTT TCCCTTTGAG ATATTCTTTC AGGTCCCGCG TACTGATGAA 2220
ACCACTGACA TCAGCTGGTC TGACGGGCCC CACAGGAGCT GACTCACCAA AGAACGCAGT 2280
TTCCACGTCC TGATTATTTC ATCCCCCTTT CCTCAACCAA TCAATGACCC CAACTTTCCA 2340
GTCCCTCACC 2350
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