| Tag | Content |
|---|
EnhancerAtlas ID | HS091-11152 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:122209460-122211320 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr12:122211054-122211067 | GAAAATTCCAGAA | - | 6.17 | | IRF1 | MA0050.2 | chr12:122210334-122210355 | CGTTTCTTTCTTTTTTTTTTT | + | 6.04 | | IRF1 | MA0050.2 | chr12:122209935-122209956 | TCTTTCTTTCTCTTTCTTTCT | + | 6.76 | | IRF1 | MA0050.2 | chr12:122209977-122209998 | TCTTTCTTTCTCTTTCTCTCT | + | 6.86 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I121772 | chr12 | 122210650 | 122211870 | | GH12I121769 | chr12 | 122207052 | 122209747 |
|
Enhancer Sequence | TGACTGTTGC CTGGATTTGG GGGAAGGGAC ATGGTTTTCT GAGACTTTCA CCAAGGGAGG 60
GCCCCAGCTG ACATCAATCA GTGCTTGCCT GTGTGGCAGG GAGACCAGAC TGGGGGAGAG 120
GGTCCCAGAA ATCCAGAAGG AGAGCTGTCC CCGCCCCAGG TCAGCTCCAC CCACCTCCCA 180
GCCCCCAGCA CTGCCTGCTC CTTCCCCAGG CTGGAACCCT GCCAACTGTG ACCTTTGGGA 240
ACTGAGTAGC ATTGGGGATA CCAGCCTTTT TTCCAGTCCT AAATAAGTCC TCCAAATGGA 300
AATATATATT ATTTTTCTCA TCTGAAAATT GCTCTGGATT TGTATACTGG TCCCAAGGGT 360
TGCCTCTGGG GAAGGGGGCT TGAATGCTTG GGGACAGGGA GAGCGTCTTA CTTTTCACCA 420
ACCTGTTTGT TCCCTTTAAA TTTTATCCCA TGTGTGTATT GCCTTTCTTT CCCTTTCTTT 480
CTTTCTCTTT CTTTCTTTCT TTTTCTTCCT TTCTTTTTCT TTCTTTCTCT TTCTCTCTCT 540
CTCTCTTTCT CTCTTTCTCT CTCTCTCTCT TTCTCTCTTT CTTTCTTTCT TTCTGATGGA 600
GTCTTGCTCT GTTGCCCAGG CTGGAGTGCA GTGGCGCGAT CTTGGCTCAC TGCAACCTCC 660
GCCTCCTGGG TTCAAACGAT TCTTCTGCCT CAGCCTCCCG GGTGGCTGGG ACTACAGGTG 720
CGCACCACCA CGCCCAGCTA ATTTTTTTTA TTTTTAATAA AGATGAGATT TCACCATGTT 780
GGTCAGGGTG GTCTGGAACT CCTGACCTCA GGTGGTCCAC CCACCTCTGC CACCCAAAGT 840
GTTGGGATTA CAGGCATGAG CCACCACGCC GTACCGTTTC TTTCTTTTTT TTTTTTTTTG 900
AGATGGAGTT TCTGTCTGTC ACCCAGGCTG GAGTGCGGTG TTGTGATCTC GGCTCACTGC 960
AACCTCCACC TCCCGGTTCA AGCGATTCTC CTGCCAAGTA GCTGGGATTA CAGGTGCCTG 1020
CCACCATGCC TGGTTACTTT TTGTATTTTG GTAGAGATGA GATTTCACCA GTTGGCCAGG 1080
CTGGTCTTGA ACTCCTGGCC TCAAGGGATC TGCCTGCCTT GGCTTCCCAA AGTGTTGGGA 1140
TTACAGGCAT GAGCCATCAC GCCTGGCTGT ATTGACTTTT CAGATACTAC AACCTACATT 1200
TTAAGTTAAA ACCTGCTTGC AAACAAATAC AAATGTATAA AGCCAAGAAT GGAAATTGTA 1260
TATCAGCCCA CCCTAGAGGT GACGTTAGTT AAGATCTATG TCCTCTCAAA AGTTTTTATT 1320
CATAAATAGG TATATACATG TGTGTATTAC ATTATGTATC TTTTACAAGT ATGGGACCTT 1380
TCTGTACATA GAGCTTTACT ATTATAACCT GCCTTTTGAA TTTTTAACAG TTTATCATGG 1440
CTATTTTTCA TGTCATTACC ACCTCATTTT TAGCAACAAC GAAGTATCCC ATTGGATGGA 1500
ACTCTGTCTT GTGTCTTAGC ATTGCACAGA GCTCCCAACA TAGCACTGGC ATAGCTTGCA 1560
TTCCAGCAAG CATCTATTGA GTGTCTACTG CATGGAAAAT TCCAGAAGTT TCAAATCTAG 1620
TTGGGGCTTA GATGGGTCCT CACATACCTG TGTTCTCTCT GTGTTCTGGA TAAGGGCTAA 1680
AGCAGGTTCA GACCAGAGTG TGTGTGTCTG TTTGTGGTGT GTGGGCGTGG GAGAGGGTTG 1740
TAACCAGGGC ACCCTTTCTG CTTCTGCCCA GTAAAGACCC ATCAGCCTGT GCTTGGGGCA 1800
GAGAGGTGTG GCCCTGTCTT CCGGGGACAC CAGGCCCTGA GCCCAGGTGC TGTGCTCCCC 1860
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