| Tag | Content |
|---|
EnhancerAtlas ID | HS018-01075 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:110044360-110045730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:110045108-110045128 | AGGATGTGGGTGGTGGGTGG | - | 6.38 | | RREB1 | MA0073.1 | chr1:110045119-110045139 | GGTGGGTGGGTGGGGGGTGT | - | 6.55 | | RREB1 | MA0073.1 | chr1:110045115-110045135 | GGGTGGTGGGTGGGTGGGGG | - | 8.93 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 110044800 | 110045479 | | chr1 | 110044516 | 110044800 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I109497 | chr1 | 110040120 | 110046097 |
|
Enhancer Sequence | CCAAGTGAGG GAGCAGTGGG AGGTAAGGGA AATGCAGCAC AAAGTACAAT CCAACTCCAG 60
TACTTGCCAA CCTGTATGTG TGCGCACATG CACGCATACA CCAGCCTTGG AGGCAATGAC 120
TCCTGCCTAA TGTATGCCAG TGCCAAAGGG CATCCAGAAG TCCCACTGCA GGGCTCCACG 180
TCCTGGCTCA CTGCAGGTTG GTTCTCTCAG GCCATGGTTC CAACCAGGGA GAGTAAACAA 240
GCTGACTAGA TTGGAGGCGT CAGGGCAGGT CTAAGTGTCT TCACCATTTT GCATTTTCCA 300
CCTAAGAGTG TAGAAGCCTG ATGAAGGGGC TTGACTGGCA GCTGCTTTAG CCTTCCTCTC 360
TCAAGCCCCA GGAGAGGAAG CATTCAGCAC AGGCTGACTG TGACTAGACC AGAAAAGCCA 420
ACCGTCCCAC TGCAGGGGCC TGAGCCTTTT CTGCTATGTG GGTGGAGAAA GTGAAGCTTC 480
CCCACTGGTT TCCTGGGAGA TACAAGATAA GTGGTGCAAG AAGTGCATGC AGAAAGGGAA 540
GGAGTTGAGA GACTGGGGGG AAGAGAGGCC AGGTTAACCA ATGCACTGAA CTCTTACCTA 600
TTCTCAAAGA AAACTGTCAT ATTAGCCTCC TCCCTCCCCG CAAGTGCTAC CTAAGAGGAG 660
CCAGGGTAAG TGCTGCAAGG CATGGCAGAC AAAATTGCAC ATCTTGGCCA GAATCTAAGG 720
AACTTCTTGT GGTTTGGGGG AGGTGGTGAG GATGTGGGTG GTGGGTGGGT GGGGGGTGTT 780
GAAGAGATGC AGCCATGGAC TTCCTTGGGC TTGGCACAGG CCAAAACAGA AGAGAGAACT 840
CCAAACTCCA AGTAGTCCTC ATCAGACTTG CTCTCCTTAT CAGCTTCATC CTGTCAGCCA 900
AATTGTCAGC CATAGAAAAA CTGCTTTGCA GATGAAAAAC TATATAAATG CAGAGTATGG 960
GAGTGCTCTG ACATCAACAG CTGTCATTTC ACTGACTGCC AAGGTTGACT TGTCTGATGT 1020
GGCTGGTTGT GCAGTAGCTC CACCCCTCGT CACCTTGGTT GTTCCTCCTG AAGTGAAAAA 1080
CAACTTTCCA AATAGAGGAG GGCTGCCCTT CGGTCAAGAC TTTAGGTAAG TATTCAAATT 1140
CGCATTCTTT TAATTTTTTT CCTGGTATCA TTTCCTCTCC CTCTTTGGAA TCTGCCACGA 1200
CAGCCCCCTT CTAGAATCAC CAAGAGAGGA GCCAAAGAAT CAGCATGGTT AGAGTTTTAG 1260
AGTCCAGTCC AATTTCTGGT AGGCTGAATC TGTACCAAAA CGTAGGGACT GCATTTTTCT 1320
GTTCCACGCA ATGCCTAGGA CACACTAAAC TGTCAAGGAA GATTAACCTG 1370
|
