| Tag | Content |
|---|
EnhancerAtlas ID | HS091-30654 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr20:33202520-33203840 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr20:33203399-33203411 | AAACAAACAATT | - | 6.22 | | HSF1 | MA0486.2 | chr20:33203388-33203401 | GAAAATTCCAGAA | - | 6.17 | | Mafb | MA0117.2 | chr20:33203070-33203082 | TGTCAGCAATTT | - | 6.37 | | NFAT5 | MA0606.1 | chr20:33203384-33203394 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr20:33203384-33203394 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr20:33203384-33203394 | AATGGAAAAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCCAAATAAG AAAAAGATCA AGCAAACCAT GAATCATTGT CTGCATCAAC ACAATATTAT 60
AAAATCACTT AAAATAACAT GCATATGGCC TATTTCAATA AATGGAATAC ACACTCAGCT 120
TTAGCAGTGC TTGTGATTAA GAAAGGCTCT GAAATCAGAC ATTTCTGGCA CTGCCACCTG 180
TACACTTTCA AGAAACATTT ATCTTGTAAG AATGGATTTG GACCATGTGG GGCCTGCATG 240
CAGTTACTTC CTCTTGAAGA AACATGTATG TACTATTCTC ATTTGAGTAG AACAAGATGA 300
TTAGAGAGCA CGCTCTGGCA TCAGATGGCC ATGGTTCATA TCTTAGCAAT GTCATTCGCT 360
GGTCCTGTGA CCTTAAGTGA CTTAACCTCC CAACATTCTA GTTTCAATTC ATTTGTCTAA 420
TATGGCTAAC ACTAGACTAA TATTTGGCTA ATAATATGAC CTACTCCATA AAGTTCTTAT 480
GAGGTTAAAA TGAGACGATG CCTACAGAGT GCTTAGCATG GTGCCTGACA TGTAATCCAT 540
TCTCAGTAAA TGTCAGCAAT TTGCATTCTT CAATTAATGT TTATTGATCA GCCACTATGT 600
TCCAAGCATT GTTTCAGATG CACATACTCC ATTTAAGTCC TATAAGAATC TTACAAGGTG 660
AGTGTTATTA TAAAGAAAAG TTAAAGAAAT GAGCTCAGAG GGGATCACTA GTTGAGAAAA 720
GAAAACTGCA AGATAGTTGC GTTTGCAAAT ATGTAAAATA AAATGCACTT ATACATTCCC 780
AAGGATATGC ATATAGTAGT GCCCCCCTTA TCTGAGGTTT CACTTTTCAT GGTTTCAGTT 840
ACCTGTTGTC AACTGTGGTC CTTAAATGGA AAATTCCAGA AACAAACAAT TCATAAGTTT 900
TAAATTGTAC ACCATTCTGA GTAGTGTGAT GAAATCTCAC GCCGTCCTGC TCTGTCCCAC 960
TCGAGACATG AATCACCCCT TTGTCTAGTG TATCCCTGCC TGTTAGTCAC TTAGTAGTTG 1020
TCTCAGTTAT TCGACAGAAA AAACATAGTA TACGTAGGGT TCAGTACCAA ATGCAGTTTC 1080
AGGCCTCCAT TAGGGGCTTT AGAACATATC CCCTGCAGAC ATGGGGAGGT CTACTGTAGT 1140
TGGGACTTAA TGATAATTAA GTCCACTTTG TTTAAAGTTA GTCAAGTTTC TATGTGTTTA 1200
TATTTTCAAC TGGGAGCAAG CTTCCCACTG CCTTTACTAA CCCGTGCCCT TCCTTTCCCC 1260
CAGCAGGGAC CAGGCCATGT ATTAAATGTC ACTTGGGTGC TGGCTTCTGA CCAGCAAGTG 1320
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