| Tag | Content |
|---|
EnhancerAtlas ID | HS091-26408 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:71172850-71174660 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:71174154-71174173 | CAGCGCCACCTTCTGCCCA | - | 6.05 |
|
| | 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 |
| GH02I070946 | chr2 | 71174101 | 71174250 |
|
Enhancer Sequence | TATATATATA TATATATATA TAGTTGTTAA CTACAGTCAT CCTATTGTGG TATAGAACAC 60
TAGAACTTAT TGCTCCTGGC TAGCTGTAAT TTTGTGCACA GATTTTTCCC TCTGCCTCCT 120
AGACTACACT TCCCCCTATT CCCTCCCTCT GACTCATCCC CAGGGTTGAG AGGTCACCTT 180
CTCCTGGATG CCTCTCCCTC TTCTCTACTT TTTGTGGTTT TATTAGTGGC ATCCACTGAG 240
GTATTTGGTC AAGATCTGGC CATGTATCTC CTCCCTACCC TTCCCCACAC ACACCGTGCC 300
CTGCTATTGG CCATGAACTG TGTTTTGTTC ATCTTCAGCT CCAGAAGCCC AACACAGCAT 360
TTTTACTGAA CACATAGGCT ATAGTAGGTG CTCAGCATGT TTGCTCAAAG GAAAGGTGAG 420
TACATTAATG AGATAAATGA ATGAATAAAT GTTAGCATGA CTAGCTATGC ACCTGTCAAA 480
ACCTGAGCCA ACAATATTAA ATAAATCAGA CCCATTCTTT GCTAACAAAC AGATTCTGAG 540
TTCATACGGA CATTACCACT TGACCCCCCA GTGTAAGGGA CGCCCCAGGA GGAAGTGTGG 600
CTGAGTAGTT AAGTGCAGCA CACTGGGTTT GGATTTTAAT CCCAGATCCA TCCCACTCTT 660
TTCTGCTAGC TACATGCCAA CCCTAGATCA ACAGCATTAG CACTGCCCAG GAACGTGTTA 720
GAAATACAAA TTCTTGGGCT CCACCTCAGA CTGACAGAAT CAGAAGCTCT GGGGGTAGGG 780
CCCAGAAGTC TGTCCTCACA AGCCTTCCAG GTGAACTGAT GCTCAAGTTA GAGAACCATC 840
AATCTCGGAT TGTAAATCCC AGTTTCCTCA TCTATTAAAT AATAATAGGA TTATTGTGAG 900
GTTCACATCA GACAAATGTA GTATTATTCT CCCTTGAGAA TAGCCAGCAA TGTTTCTGCC 960
TGGAATGCAG AAATGCTAAT AAGCCTGATT CAACAGTTGG TGCCACCTCC TGCCCCCTCT 1020
CCACCTCCAC CACACTCTCC ACCAGACCTG CCATTCTCCA TGGGACCCAG TGTGGCATGG 1080
AGTCGGAACC TATACAGGTG TCCATTTTCT CCACTGTAAA ATGAGGCCGA TCTAGGAAAC 1140
CAGAACTAGG TCCCCAGACC TGTGGTTTTG CGACTATCGG ATGCATCTGT AGCTTTGGCA 1200
GAGAAAAATA ATTGGGTGGT GGAGGCACCT CTCCCCATCC CTCTCCGTTG CCCCTACCCC 1260
TTTCCCTCTA CCAGGATTTG GCAAATGCTA CAATTCTGTT TCTACAGCGC CACCTTCTGC 1320
CCACATTGAA TCACACAGGC AATTACTCTT CCTGCTTCCG TCCTCAAATG TAAGAACATT 1380
TGAGGGAAGA ATTTTGTGTA GATCAGAGGT TCTTAGCCCA AGGAATTAGG CCCTTGAAAT 1440
TGTGTGCAGA CCTTTGAAGG TATGCATGAA TGTGCCTGTG CATTTTTCTG GTAGGAGTTT 1500
CTACAGTTTC GTCTGATTTT TCAGGGTTCG TGACCCAGAA AAGTCTAACT CTCTGATTTG 1560
TATAAGTTGA ACAAGCATCA GAATATCAGG GGTGCAGGGG GCTTGTTAAC AGGCAGATTG 1620
CTAGGCCCCA CCCCAGAGCT CTGATTCAGC ATGCCTGGGG TAGGAGGCCC AAGAATGTAC 1680
ATTTCTATCA AGTTCCTAGG TGATGCTGCT GGTATGGGGA CCACACGGAG AACCTCTGTT 1740
CTAGAGAATC TTCTGACTCC TGTAGTCTGT GATTCAAATT GGTCCCTGTT TGAGAATTGG 1800
AGTAAGCACT 1810
|
