| Tag | Content |
|---|
EnhancerAtlas ID | HS118-15337 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr5:131698940-131700400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr5:131700179-131700190 | TATTGTGCAAT | - | 6.62 |
|
| | 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 |
| GH05I132362 | chr5 | 131698145 | 131702697 |
|
Enhancer Sequence | TAGCCAGGTG TGGTGCGTGT AGTCCTAGCT TCTGGGGAAG ATGAGGTGTG AGGATCACTT 60
AAGCCCAGGA GGCAGAAGTT GCAGAGAGTC AAGATCATGC CACTGCACTC CAGCCTGGGT 120
GACAGTGAGA CCCTGTCTCA AAAAAGAAAA AATATTCTGA TAGTGTTCCA TCTAGAATAA 180
AATCCAAACT CCTTGCCACT ATCTACAAGG CACTAGACAA TTTGGCTTCC ATAAAAACTG 240
GCCTCCTGCC AATGTCTCTG ACTTATGTTC CAACATTACT CACTTTGATC ACTATGTTCT 300
AGTCACGCTG GTCTTCTCTC CGTTACTTAG TCACCCCGAG CACATCCCTT ACCTCACAGT 360
CTTTGTACTT GCTGCTCTTC TGCTTAGTAC ACCTGCTTCC CAGATCTTCA CATGACAGAT 420
TCCTTCTCGT CCTTTGCCTC TCAGCTCAGA TATCACTTTC TCAGAAACAT GTTCACTTAC 480
CATTCATCTA AAGCAGCTAC CCAATGACTG TCATTCTATA CCATTACTCT CTTTTCTTTC 540
ACCTTGGCAA TTACCACTAC TTGAAGTTTG TATTTATTTG TACAAGTTTA TTGTCAGCCT 600
CTCCATCCTC CAAGTAAAAT ACGAGCTCCA TGAAAACAGA TAGCTTGTTT CTTTCCTCAG 660
TTCCCAGAAC TCGGAACAGT GTTTGGCACA CATCAGTCTA TTCATATGTT TGCCAAATGA 720
ACGAAGAAGT AAAAACCACT AGTGACCCAA TTTTCCTGCC ATGTCATATA TATACATAAA 780
AGTCTTTTGG GAAAACTCAT ATTTCTATAT TGGCCCTCAC TAATGTCTTT TCCATCTATT 840
CTAGAATGCA ATAACCAGTC TTTAAAATGC AAGCAGAATA TTTCACATTT CATTTTTGCA 900
GGTATCTCTG AGGGGAATGA ATTTACATTT CTACTACCAC AAATAGGATG GTCAAGTTTG 960
TTGCAATGCA AAATTTTTTC TGTGGAATTC AAAAACTGTC CTGTACCTCT TGAAGCCGAA 1020
TTGTGGGGTT TCACATTGGA AATTACACTC ATCTAAAGAA ACAGTCTGGA CATTTAAGTC 1080
CTTAAACAGT TGTTCAAAGT ATTTTATTAC ATACTTTTTC TAGTCTTCAG AATGTTTCAA 1140
GGTCCATTGT CTTCATGGCT AGTTACCTGT CTGTCCAGGC CAAACAAACT GGAGTTAAAA 1200
TGCAGAATCA CATAACAGCA GAAATGTGAT TTCTCATTCT ATTGTGCAAT CCAACAGAAT 1260
TGTGCCAAGT CTTGCTAGGC TGACGCTGCT CTACTCTGCC CAAATGCCAA TATGCATTGG 1320
GGTGATGACA TCCCACTTGG GATATTGTCT GATGACACAG ACAGACTTCT CTGTTTCTCC 1380
ACTCTTGGGT CATATAATTC AATGTTCTGG GGCTGAGGCA AATAATGTCT TACAGTGATT 1440
TTGGCAAGAA AAAAACAGCT 1460
|
