| Tag | Content |
|---|
EnhancerAtlas ID | HS091-28929 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:218938610-218939810 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr2:218939725-218939736 | TGATTAGATTA | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCCTCTGCCC TGCCTTCACT CTGAGTTGCC TCTTCCCCAT CTCCTTGGCA TCCTCAAGTT 60
GAGTAGAAAC TGAGCTTCCC CCTCCGAGTG TACAGAGAGC CCTGACCCTA CAGGACAGAC 120
AGAGCAAGAG GCCAGTGTGT GGAGCAGGGG ACTGGGGAGC TGCAGAGGAG GAGAGGGCTC 180
CTATTCCTGG GGTGGCGGGG ACACTGGGAG AGAAAGGGAA CTCTAGCACC CTCTGCCGGA 240
GCCACTGGGC CCAGACAAGG AGAAAGTGCT ATGAGGGGCG GGCCACTGAA AGCTTCAGGA 300
AACAGATGAG AGGGACACCC TCTGCTGAGT CCCCTGCACT GGACAATTGA CACATGACTC 360
AGTTCAGTTC AAGAAGTGAC TAAAGACCCA GGTTGCCCGG TTGAATTCCA GCCCCACCCC 420
TTACAAACTG TGGTTCTTGA ACAAGTTACT TGTCCTGCCC CATAGGGATA TTGTGAGGAT 480
GAACGGACAC AACTCACATC CAGCACTGCA CAGGGCTCCT GGCTACACGC TCCCCGCATG 540
ACAGTGTGTG GTCACCGTCG TTGTTATCAT CATCCCCCAA GCACATTTTG CACCCCCACC 600
AGCTTCCAGG CACTGGGTAC AGATACTATT AGTTCTCTGG TCCGAAAAGT TCAGGGTCTC 660
TTCATGGAGA TATACCATAA AAAAAAGCAT TGCAATATAC AATTTCAGTG TAAGTGACAC 720
AGAAATGAAC AGAGGAACAT GGGAGCACAG AGGCTTCTTG AGAGGTTGCT CTTAGCTGAG 780
TGTCGGTCTA GTCGAGATTT CATCACAACC CTAAAACCGG GTATTATCAT TCCCATTTTG 840
CAGATGAAAA AACTGAAACA TGACATGTAG TTCGGGAGGA AAAATTAAAG GAAAGGAGTG 900
AGAGGAACTT AGGGGGAACC AGATCAATAC CCAAGACCCA GGTGCAGGAG GGAGAAGGAT 960
GTGGGCTGCG GGAAGGGACA GAAGGACATC AGGATGTCCC TCACCAGACC AAAGCATGGC 1020
GCTCAGATCA CCTGGGTGTT GCTAAAAGTC AGATTTGGGG TTTGATAAAT CAAAGCTTCC 1080
AGTGAGAGGA CCTGGTACCT ATCTATTTAG CAAGCTGATT AGATTAGCAC TGTGGCCTAA 1140
TCTAATGGCA CCAGGTCAGT GAATTGGTGC TGAGAGGGAT GACTGGTTTT GGGTCCTCTC 1200
|
