| Tag | Content |
|---|
EnhancerAtlas ID | HS091-00932 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:26504090-26506280 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr1:26506124-26506134 | GACATATGTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGGGTGGGG CTGGGGTAGA GTTGGGCTTG AAGGGGACTA GGTGTGGTGT CCCACCGGGA 60
AGCGGGAGGA GAGGAAAAGG AAAAAAAATC TGCGGACTGG GTGCGCTGGT TCACACCTGT 120
AATCCCAGCA CTTTGGGAAG CCAAGGTGGG TGGGTCACCT GAGGTCGGGA GTTCAAGACC 180
AGCATGGTGA AACCCCGTCT CTACTAAAAA TACAAAAATT ATCTGGGGGT GGTGGCAGGT 240
GCCTGTAATC CCAGCTACTT GGGAGGCTGA GGCAGGAGAA TCGCTTGAAC CCAGGAGGCA 300
GAGGTTACAG TGAGCCGAGA TTGCACCGCT GCACTCCAGT CTGGACGACA GAGCGAGATT 360
CAGCTCAAAA GAAAAAAAAA AATAATAAAC TGCGGGCTCT ATCAGTCGGT CAGTCAGTCA 420
ACAAATATTT ACAGAGCACC TAACATGTTC CAGGAACCGT GCTGGGCAGA GAGACAGATG 480
AGATGACCCT GGGGGGCCCA AGGACCCAGA AGGGGGCCCC TCATCATGGC AGTAGCCCAA 540
GAGGCCTCTA GGGTGATAAT GGGGAGGCGG TGTCATGAAA ACAGGAGGGA GGCCTGACAG 600
GCCCACACCC ACTGTATCTC CTTCATCTTC CCTGGCCCCA GGGCCAGTGG GCTGTTGTTA 660
AATCCGTTTC TTAGAGTCAG AAACTGACAC ACAGAGCCAG GAAATGATTT GCTCAGTCTC 720
TGGTGTCATT TTCCCCGCTC CACACCCTGA GCTCCTAGTG ACAGAAGCAG AAGCCCTAGG 780
CCAGACTGAA GAGGTTGACA CAGCCCCACC CTGGGGCTCC TATCCAAGGG GCAAGGTGCT 840
GTCCAGGCTC AGCGAGCCCA CACAGATGGG AAGCAACACA CCCCACAGGC AGACTCAGAG 900
AAGGAAGGGC CTCCTGACAC ACAGTGCGAC CAGGAGCAGG CAGTCAGGAC ACCCCTCCCA 960
GAGTGGGGAG CTGGAGCGCA CTAGAGACAG GCTCAGGAGG ACCAGCCCGG GTAAGGGCAG 1020
GAATTCAGGG CTGGGTTCAG ACTCCCAGGC TGGATTCCAG GCCCACCCCC ACCGCTTGCC 1080
AGCTCTGTGA CCATAGGTCT TAGTTTTTCT GTCCATCAAA TGGGAAAGGC AACTCTGACC 1140
TTATGAAGTC GACAAAGTGA GACAATCATG ACATAGTTCA TTTGTAGCTC AATGCCTGGG 1200
TCTATTGGGA GGGCACCAGC CCAATACAGT CACCGTGCAG GAAGGAGGTG GCTCAGGGGC 1260
CCATAGCCAG GGAGTGATAG GTTCATGAAC TCCCAGTCCA GTGCTCTCAA TGTGACACAG 1320
GGAACACACA CACACACCTC CCCCAGTGAA GGAGCCTGGC TTAGAAGGGG AAGAATTCCT 1380
TCGAAGAGTG AGCAAGCTAC TTAACCTCTG TGTCAGTTTT CCCATCTGTA AGCAGGATAA 1440
TGATAGTCTT TACCTCCTAG AAATGCAGTG AGAATCAAAT GTGTTAATAT GTGTAAAGCT 1500
CTTATAGATT TGCATAGCAC ATAGTAAGCC CTCAATAGAC ACTTTTCTTA TTTTTCAGTG 1560
CCTACCTTGT CCAGGCACAG GCCGGGGGTT AGAGACAAAT GGTTATCTAA GGCCTGATCT 1620
TTGAAGAGCC TGTGATAAAA TGGGAAAGAC CGATGGTCAA GTGCAGGGGT TTGTGGAGGC 1680
TCAGGGGCAG TGGGAACAAG AGGAGAGCCC TCCATCCCAC TCAGCCTGGG AAGTTATGGA 1740
AGGCTTCCTG GAGGAAGTTA GATGAAAAAG GAAGTGAAGG AGATAGAAGA GCAACGCCAG 1800
CAGGAGGAAT AGCACTTGCA AGGACGCTGA GGTAAAAGGG TGTTCCAGGA GCTGCAAGGA 1860
ATTAGCTCTG TGCATCTGAA ATGTTGAGTT TAGGGGGCTC TTCAGGATAT GATGCTGGAA 1920
AGGGAGGTAG TAGCCTAATC ATACAGGGCC TGTAGGTCAT GGTAAAGTCT GGCAATAATA 1980
ATATGATGGC TATTATTGGC TGTCTCCCAC GAACCAGACA GTGGCCAAGG CCTTGACATA 2040
TGTTGTGTCA TTCAATACAC ACATGATTAG AAGGTAGGTA CTTTTATTAT TCTCACATTA 2100
CAGGTGAGAA AACTGGGCAC AGAGCAGTGC TATTACTTGC TCAAGTGTTC ACAGTGTCTC 2160
AGTGACTCCA TAGCCTCTTG TTCTTATCCC 2190
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