| Tag | Content |
|---|
EnhancerAtlas ID | HS059-04095 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr1:212839840-212841360 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr1:212840971-212840988 | TGAGTTCCTGGAAAACA | - | 6.28 | | POU2F2 | MA0507.1 | chr1:212840708-212840721 | ATATGCAAATGAA | - | 7.82 | | RREB1 | MA0073.1 | chr1:212840729-212840749 | GGTGTGAGGGTGGCTTGGGG | - | 6.51 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCGGGTGGT GCCCAGCTTT CAGTGGTGAG ACCTGTAGCC TTTTGCTCTC TGCTAGGCCA 60
GGGAGCCCCT TCTGAGAGGG TAAGGGGGGC CAGGGTGGAA GGGGCATGGT TCTTGTTTTG 120
TGTCCTGGAG AGAGTGTGCT CCATATAAAG CCTGCTTGAG CAGAGGAGAA GAAGCCGGCC 180
CCGGCACCTT AGCCTTGACC CAGGTTCGTA TGGTGTGGAG CCCTTGCTTC TGCTGTGATC 240
GGGCCCAAAA GGTTAACAAG TCAGTTTGTA GAGGTCTGTG TCTGGGAGTT CTTTGGGGTT 300
TTTATTTGTG TCTTTCCTGA CTTTTCTATC TCTGAGAGTC AAGTCTTTCT TCCACATCTC 360
TGTCTTGCAC TGCAGTTCCC CAGTGCGCAA TCATTCCATG TGTGTTGACG GACTGCAGGG 420
CACATTGGCT CTGAAGGCTT TACCAAGCTG GCTCTCAGTC ATATATATAT TTTTTTAATT 480
TTTGAGACAG GGTCTCACTC TGTTGCCCAG GCTGGAGTGC AGTGGCACAA TCATGGCTCA 540
TAGCAGGCTC GAACTCTGGG GTTCAAGCGA TCCTCCCACC TCAGTCTTCT GAGTAGTTGG 600
GACTACAGGT GCCTGCCACC ACACCTGGCT AATTTTTATT TTATATTTTA GAGATGGGGA 660
TCTCATCATG TTGCCTGGAG CTGATCTCAA ACTCCTGTGC TCAATCAATC CTCCCTCCTA 720
GGCCTCCCAA AGCGCTGGGA TTGCAGGAGT GAGCCAACAA ACCTGGCCTC AATCAGGTCT 780
TTAACCGTCC AATTTATTCA ATTCTGCCAG AGGGCCCCCT GCTGAAGCTG TTCACAGATT 840
GCTCTGATAT CATTAAAAAG CTAACCACAT ATGCAAATGA AGTGTTGGAG GTGTGAGGGT 900
GGCTTGGGGT AGACAGTGCT TCTGGTTCAT CTAGGAAGGC TTCCTGGTGG GGGAAGGGGA 960
GGGGCTGAAG TTGTCATTGA AAAGGATGGA GTTTGATACA ATGAGGGGGG TGGTGTGGTT 1020
TTAGGCCATA ACCCTCCCTT TCCTGGGGCA GGTCCTCACA TGAGTCATTC CAGAGTTCCC 1080
TTGCTGGTCA GTGGGAACAT TCTAGTGTGT GACATCTCCC TGGCAACAAG CTGAGTTCCT 1140
GGAAAACAAC AATCACAGAG AGACAGTCCA CCACCTCTAC CCTCTTAACT CTTCCTTAGA 1200
AATCCTACTG TCTGCAGCTG GGAATGAATG GAATGAAGGT CAAGGATGAA GTAATAACCA 1260
AATATTGGGT TTTGGGTGCC CTGGTAACTG TCCGGTTTCC AGTTAGGGTT CCTGGGTGAC 1320
ATCTTCCTTC TGGGGGAAGA CAGAGTCAAA TGAGAAACGT GAGTTGAGCC CAGGGGAAAG 1380
GATCATCCGG GAGATGCCTG AGGGGCTCCA GGGCATCGTA ATCTCTTGCT CAGCTGGCAG 1440
AGTGGGGCTG ACACGGCCAG CTGCTCTCTG GAGTCCTCGG CCTTCCTGTT TCCCCCTGAG 1500
GACTTTGAGT GGGGAATCTA 1520
|
| |
|
|
|
