| Tag | Content |
|---|
EnhancerAtlas ID | HS091-13662 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:74759950-74761850 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr14:74760360-74760372 | AAATAAACATAC | - | 6.11 | | NKX2-5 | MA0063.2 | chr14:74761139-74761149 | CTCAAGTGGT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr14:74760976-74760991 | CGAACTCTTGACCTC | - | 6.24 | | RREB1 | MA0073.1 | chr14:74761091-74761111 | CCACCTCACAACCCCACCCC | + | 6.12 | | ZNF263 | MA0528.1 | chr14:74761698-74761719 | AGGGCAGGGGGAGGTAGAGGG | + | 6.01 | | ZNF263 | MA0528.1 | chr14:74761704-74761725 | GGGGGAGGTAGAGGGAGAGGG | + | 7.11 | | Zfx | MA0146.2 | chr14:74761001-74761015 | 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 |
| GH14I074293 | chr14 | 74760581 | 74763780 |
|
Enhancer Sequence | TCTGACAAGG AAAGGCTGGG ATGTCCACAG GGCTGGAGAG GTTCAGCCAG GTTGGGGGGC 60
CGCCTGTCCC ATATCACACC CTCCTTTAGA AACCAAGGCC ATTCAAATGA TCTTGGTCTC 120
AGGATCTGTC TACTGGTAGC GCCCATTCAC GGCTTCAGTC ATGCCTTAAT GGTATTGTCT 180
GTGTGAAGAA CATAAACTCT AGAGTTGGGC AGACCTAGTT CAAATCCTGG CTCTGGCCAG 240
TTACTAGCTG CGTGACACAG GCAGGCTACT TAAGCCTCCA AGCCTCAGTT TTTTTAATCT 300
ATAAAATGGA GCCAATAATA CCTATGTAAT AGGTTAGAGT TAGAATTAAA AGTTTCTAAA 360
TATAAAGTGC CAAGCACATA AGGAGCCCTC AATAAATAAA AACTATTGTT AAATAAACAT 420
ACACAGAGCG GTCACTAGGT GTACCAGGCA TTGCACTAGT TAGCTAGTGC AATAAAGAAA 480
TGAGAAAATT ATCTCTGTCT TTGAGGAGCT CTCAGTCCAG AGGGCAGGCA GGCACACTGC 540
ATTCTTCACT TGGAATCAGG AGTACTAAGT GTGCCCTCAG GGCCATGGCA GCAGATAGGC 600
TTAGCCATTA AGGGAGTCTG GGAAGGCTCT CCAGAGGAGG TGATCTGGGG TTTCAAGGAT 660
GGGAAGAAAT TCGCTAGGCA GAAAAGGTGG AGGGAGATTT CAGATTTTGC ACAGAGGCCA 720
CAGAAGAACT CATCTGAAAC TCTACAAACT AACCTGCCTT CCCCAGAGCT TCATGAGCAG 780
AGGCTGCAGA ATCCAAAAGC AACTTTTTTC TTTTTTTTTT TTTGAGACGG AGTCTTGCTC 840
TGTCACCCAG GCTGGAGTGC AATGGCAGGA TCTTGCCTTA CTGCAACCTC TGCCTCCCGG 900
ATTCAAGTGA TTCTCCTGCC TCAGCCTCCC CAGTAGCTGG GATTACAGGT GCCCGCCACC 960
ATGCTCAGCT AATTTTTTGT ATTTTTAGTA GAGACAGGGT TTCACCATGT TGGCCATGGC 1020
TGGTCTCGAA CTCTTGACCT CAGGCAATCC ACCCGCCTCG GCCTCCCAAA GTGCTGGGAT 1080
TACAGGCATG AGCCACCATG CCCGGCCTCC AAAAGCAACT TTTTTACACA CCCAGCCCTG 1140
CCCACCTCAC AACCCCACCC CAGCGCAGAT TCCCAGTATT CTTGGTGCCC TCAAGTGGTG 1200
GAGGTTGCAA ACTGCAGCAG AGACTGAGGA GCAAAGGTCC CAGGGCTATC ACATCCACCC 1260
CAAGTACAGA GCCAAGGAGT AGCTTCCACT TCTTAAACGC AAACCTCTGC CTGCACTATC 1320
AATCCTAACG CTGATTTCAG AGGCCTCACA TAAGGCAGAG CACAGGGACC GGTTCTGGCC 1380
CTGGAGGGAA GGGATGGGAT TTCATGCCGC TGCTGCTGCT CCTGCTGCTG CCGTCAGGAG 1440
ACCAGACGCT TGGCTCCATT AGACAGCATT GTGGGGAGCA GGTCTCCTGG TTTTCTGAGA 1500
AGCTCCCATT CCATCCCACG CTACGGAGAC AAAGGATCAG GCTTGAACCT CAGGCACTGG 1560
CAAGAAAGCT TCTTAACAGA CAGAAGAGCA GAGGCAGACG GATGTCTTAC AGTCACCAGC 1620
AAGAGGATGA GGCATTCATT CATTTGACAA TTTCAGGCCC CACGCTAGGC CACTAAGACT 1680
AAAGCTGGCC ACAGTAAGGA ACCACCAGCT TCAGAAGCAA ACCCCTGGAC CTAAGGATGA 1740
GGCAGGCAAG GGCAGGGGGA GGTAGAGGGA GAGGGTCACA GCCAAGTGTG ACAACACTCA 1800
GCCCCTGAGC TCGGTGGTGG TGGGAGGGTT GAGGATTCAT CTTTCCTTCT CCACTCTCAG 1860
CTCTGGCAAG GCAGAAGGGG AACCATCTCT CCAGACTCAC 1900
|
