| Tag | Content |
|---|
EnhancerAtlas ID | HS010-02794 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr20:39620000-39620970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr20:39620581-39620602 | GAAGGAGGAAGGAGCAGAAGC | + | 6.21 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_34557 | chr20:39619000-39620249 | HCT-116 | | SE_34892 | chr20:39619063-39621042 | HeLa | | SE_59160 | chr20:39597141-39642711 | Ly3 |
|
| | 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 |
| GH20I040990 | chr20 | 39618801 | 39621248 |
|
Enhancer Sequence | GCAGTGAGGT GTTCACATCA TCTCTACAGA AACAAACAGA ACAGAGCAGG GAAACTTCCT 60
CTGGGTCTGT GGCACCCAGC TCCCCAGACC TTGCAATTCT GGAGGAAGCC TCAGACAAGG 120
CTTTTTGTGG GGTGGGTGTG GGAACCTGAG TAGGACTGAG AGCTGGAGGT TTCAGGGCTG 180
GGAGGGCTGC ATGACAGAAG GTGCTATTAG CCCAGCTCAT GAACACTGAG CAGTTCCACT 240
TCCCCCTTTT CAAAGTAAGC ATGGTGGGGG AGGGAAGAGA CAGGCCTTGT ATCACCCCTT 300
GATAGGCCCA GGGACCTAGC TATTAAAAAC AGGAAATATG AGCCAGCAGA GAGTAAGGAG 360
GAACTAACTG GGGGTGCCCT GTCTGCCTCC AACTACAGGG AGCCTGCCAG CTACCTTAAT 420
TCAGTCTAGG CAGATGACAG AGAACGAATA GACCAGCTTG ACTGAAGCCT CCTGAGAGCC 480
TGGGAAGGAG ACCCAGGACA TGAGTCTGGG CATGACTTTG GAGGAGCAGG TTGTAAGAAA 540
GGGGATAAAG AGCTAGAGCT GCAGGCAGCT ACTCCCTAGA GGAAGGAGGA AGGAGCAGAA 600
GCCTGAGACA CAGACTTGGA TGGCCGTGTG GATGTGAGCA GCTGTCCAGG ACCTTCAGAG 660
GACCAGTTTG AGCCCATTTA TTGGGAACCA AAAATGAGGA TATCAGGATG GACCTCCAGC 720
ACCAGGGTTT ACACTCTGCC ACCCACTATG CACGGCCAAT CAACATTCCC AGCACTGTCC 780
AATAGAACAG TGCAATGCTG AAAATTTCTA TAGCTAGGTT TTCCAATTTG GTAGTCATCG 840
GACTCATGTA GCTAGTGGCT ACCATATTGG ACATCAGAGC TCTAGCCCCA TGTGTAAGGT 900
GAACAAAGAG CTGCCTTCCA ATATTTCTTT TATTCCCTCC CACTCCTTCC ATTCTTTCAC 960
ACCCTCCTCT 970
|
