| Tag | Content |
|---|
EnhancerAtlas ID | HS091-26471 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:73247390-73249650 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB18 | MA0698.1 | chr2:73249570-73249583 | GCACATCTGGATG | - | 6.82 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 73247583 | 73249377 | | chr2 | 73248054 | 73248385 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I073020 | chr2 | 73247480 | 73249172 |
|
Enhancer Sequence | AACCTGTGAA CGAGAAGAAA AGAGTCAGGC CTTATAATCC ACTCACATCT CACCTGAGAT 60
ACCCAGGAGC CTCCGGGTTA GGTCTTAGGC TATCAGTGGC CCTGATGAAG GGGCTCAGGT 120
CAGTTAGGCG GGAGGCATCT CCTATCTCAT AGACCCTTTC CCAGTTCAGC CCTCACCGGG 180
GCTGTGTCCC CAGCCTCCTC TTCTCTGCTC CCCTTTGGCC AGGCAGCTTT CACTCTCCCC 240
TGGAACCCAG AGGCCTGTTC CTGCAGGCAG GGCTGCCTGC GACCTGGGGC ACCACCACTC 300
CACACTTGGT GATCCTCCTA CGATTTCCTG CGAGGCACGA CACACCCTGC CCACGCTCAC 360
TACATGAGGC TGAACATCCT CCAAGGACCC CAGAATGTCT TCCTTCTTGC CTCAGCTTGT 420
CTTTCTAACA CAGGCCCTTA CTTCCCCGGC ATCATGGCCA TTTCTGGAAA GAAAATTCCC 480
TCCCAAACTG AGCCATGCAC CTCTAAGTGC CAGAGCTTCT TAAATCCGTG GCATCCCCAG 540
TGGCGCAGTA GGGAGCTGGG GTGAAGCGCA GCCAGGCTGT GAGTACAGCC TCCTCGCTGC 600
TCTCAGCCCC CAGGCGAGGC TCTCTCCACA GCCCCAACTG CTGTCAGTGG ACAGCCTCCT 660
GTCCCCAACC TCTAACCGTG GCAGCCAGTG AGCAGTGGCT GGACAGCGGG ATCGGGCTTA 720
TCTGACTTGC ATCTAAAGTA AAGCTTTGCT CCTGAGTGCA CATAATCACA CACACACGTG 780
AGCCATGGTT CTCATACCCA CTTCTCTCTG GGGAGAGAAC CAGAGTTTGA TCAGGGCCTC 840
AGAGGAATGC ATGACTCAAA AAGGTCAAGA ATTACAAGAG AAGCCAGGCT CAGGGTGAGA 900
GCCTGCTGTG CCGGGTGCAG GGACTGGGAA GCATCTACAA CCACAACTGT AAGATGCTCA 960
GAGCCCTTCC CAGCACTTTG GGAGGCCAAA GCAGGCGGAT CACTTGAGGT CAGGAGTTCT 1020
AGACCAGCCT GGCCAACATG ATGAAACCCC ATCTCTACTA AAAAATACAA AAATTAGCCA 1080
GGTGTGGTAG TGTGTGCCTG CAGTCCCAGC TACTCGGGAG GCTGAGGCAG GAGAATCGCT 1140
TGAATCTGGG AGGTGGAGGT TGCAATGAGC AGAGATCATG CTACTGCACT CCAGCCTGGG 1200
CAAAAGAGGG AGACTCTGTC TCAAATAAAA AGAAAGAAAA ATGCTCAGAG CCTTAAAGTT 1260
CTTCACGGCA AAGCCAGGGG GTCACAGGGC ACTCACTGCC CCAGTTTACA CAATGACATC 1320
ACATGTCCAT CAACTTCCTG GTTGTTTATT TTCTTGCCCT CAGTGAGGCC AGGCTCTCTG 1380
GGGGTGGCGA CCCTGAGGGA CCCATTTGAC TGAGACCGCC TTTCTCCAGC CACCCGAGGC 1440
CTTCCCAAGG CAGCAGCAGC AGTGCCCTCC CATTCCACCC TCATAATTCA AGGTGGCTGT 1500
GCCCCATTGC ACTGAGAAAT GGCAAGAAGG AGGCGTCAGC ACACCCATGA GTGTGACTCT 1560
GCAGAGTCTC TCACAACTGC TGGGGGGATA AGCATGCCAG CCTAGCTCGT GTACATGCCA 1620
GTGCTTTCTA AGCCCTAAAG CCCACATAGG CACAGCTGCC CCTTCAGTGA CCAGTGGGAT 1680
TTCCTGGGGC AGGGATCTTG TATCACCCTC TGCCTCCTGG TCTCCACAGA ACAGGAATCC 1740
CACCTTCTGT ATGTGCACAG CAGTGCAACA ACAGTGCATC CATTCTGAAG GGAGGGCTAA 1800
TGGCAGGATC AGAGAACAGA GAATTAGGCT GGAGACTGAC TGCCTAAAAG GGGCAGGGCA 1860
GGGAGCAGGA CTTGGAAGGA AACAGCAGGT CACACACCGG TGAGAGGGGG AATGACTTGC 1920
AGAAGCCAGG GCTTGCTTAC AGCAGGCATC ACTGAGGCTG TCCTAGTGTG CGCTGAGTGA 1980
TGTGGAGTGG GTGGTGGTGG GGGCTACCAG ATTCACCTGT GGAAGCCCTG GTTCCACCCC 2040
AACTGCTCAG GCAGAAAAGG CAGGTAAGCT CCATAGAGTA TTCTGAGGCC TGGCCAGCGC 2100
CTTGTACAGT TGAGCTGAGG TGAATGTAGA GGTGCAAATA TGGCCATGAT TGTAACAGGC 2160
TCTGTCCCCT CCTTAGGCCA GCACATCTGG ATGCTCCTGG AACTGTGACT GGAGTAAGCA 2220
CCCCAGGCTG ACCAGAACCA GAAGGGCCCC AGGAGCTTAC 2260
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