| Tag | Content |
|---|
EnhancerAtlas ID | HS091-38469 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:73838800-73840280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr5:73838990-73839001 | GCAGGGTGTGG | - | 6.62 | | RARA(var.2) | MA0730.1 | chr5:73838947-73838964 | ACGTCATGGAGAGGTCA | + | 6.17 |
|
| | 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 |
| GH05I074542 | chr5 | 73838079 | 73840937 |
|
Enhancer Sequence | TATTTTGAAG GCACACAGGA GCTTTTCTTT AACCCAAGAG TGGCACCCTG TTATAGATAT 60
TCTCCAGTGA CCCAACTCCC ATCCCCTCGC TTTTCTATAA AAGGAGCCTG GAGTTATAAG 120
AAAGACAGGA CAGCCCTCCA AACCAGGACG TCATGGAGAG GTCAGCCCAC CCAAAGAAGA 180
TGCAGCACAT GCAGGGTGTG GAGAGGGAAG TTCACGGGTG ACGGGAGACA CTGCCCTACG 240
CCGCTAAATC CCTGCAGCCT CCTCCCCCTC ATCCCTGTAA AAGTGAGTCA GAAGAGCTCA 300
CTTGTCAGAC TCCTCCCAGC CCAGAGTTGA AACAAGCTTT CCCCCACTCC ATGCTCCACA 360
AGCCACAATG CTCCAAGCCT CCTCAAATTC ATCCATGAAG CTCTGTGGGG CCTGCAGGCA 420
GGCACATTCC AAAAAAAGAC CTGAATATTT TATTGACAGT GGAACCCTAA TTAGGTGGTT 480
TCTATAGTCG CCGATTTCTC TAGCACTTGA AGGCAGAAGT CAGCGTTTTT GTCCCCTTCT 540
AATTTGCCCT CTCTACCCCT CACACTCCAG ACCCAGGGCT GCTGGCACCC CTGCTGAGAA 600
GAATAGATGG GGAAGAAATA TTTCCGGGAT TAGTCTCATA AATCTTTCAC TGGCTTCCCT 660
GGAAATTCTC TACCCTTGAG CAACGGGGGT GTGGGGTGAG GGGAGGAGTC AGATCACTCC 720
TGACTCATTA GCGTGTTTCC ACGATGTGCC AGCTAGATCA TCTAAAAATT ATTCAGCTGC 780
CCAGGAGGAA AGCCTTTTTG CCAAACTACA GGCTTATTCG AAGAACTTAA TGCAATCCTC 840
AGCCCTGGCA TCCAACCACA AAGCCCAGCA AGCTCTTCAG AGAGCCATTT CCTGACCCCA 900
GAGGCAGTCA GTGACCCCCT GGAGTGGATT TTTACATAGA GATACTGTCC TTAGCCGCAA 960
AGCTTTCTAA AGAAGGGATT TGGGAAAGAA AATCTATTGT GTTGTTGGCT TTGTGCGTGT 1020
CTGAAAGAAG AGAAGTCATA AAATCTTTGT GTTCTTGATG GAGTGAGTTC CAGGAAATAT 1080
TACCTTTCCC TTATCAGGTC CCCATGAATT GAATCAGGCT GATAACATAG CCTTCAGGTT 1140
TCCACGTGTG CATTCACCAC CTACATTTGC AAAAACTCTT CCTTTTTCTG TTTTGTCCTC 1200
TCTCATATCT AAAAGATTTT ATCAGCACTT TCTTGCTGTA TCTGTGTCTG TTTTCAGTCC 1260
CTTGTTGGTG TTCTACGTGG TATGTCCAAT TTTATTAATA GCAGGAGGCC GGGTGTGGTG 1320
GCTCATGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGCA GGTGGATCAC TTGAGGCCAA 1380
GAGTTCAAGA CCAGCCTGGC CAACATGGTG AAACCCTGTC TCTACTAAAA ATACAAAAAA 1440
TTACCTGGGT GTGATGGCAC ATGCCTGTAG TCCCAGCTAC 1480
|
