| Tag | Content |
|---|
EnhancerAtlas ID | HS018-01968 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:206939360-206940650 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PBX1 | MA0070.1 | chr1:206939368-206939380 | ACATCAATCAAT | + | 6.44 | | TCF7L2 | MA0523.1 | chr1:206939770-206939784 | TCGCTTTGATGTTT | - | 6.54 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_18640 | chr1:206938558-206940480 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19631 | chr1:206939257-206940450 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_61266 | chr1:206939355-206991151 | HBL1 |
|
| | 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 |
| GH01I206765 | chr1 | 206939241 | 206940345 |
|
Enhancer Sequence | GACATGAGAC ATCAATCAAT ATATGTAAGA AGTACATTGG TTCCATCCAG AAAGATGGGG 60
ACAACTCAAA GCAGGGAAGG GGCTTCCAGG TCACAGGTAG GTAAGAGACA AATGGTTGCA 120
TTCTTTTGAG TTTCTGATTC TTTTCCAAAG GAGGCTATCA GATATGCATC TATCTCAGTG 180
AACAGAGGGA TGACTTTGAA TAGAATGGGA GGCAGGTTTG CCCTGAGTAG TTCCCAGCTT 240
GACTTTTCCC TTTAGCTTGG TGATTTTGAG GCCCCAAGAT TTTCCTTTCA CAGACTCAGG 300
ATGTCTTCTT CAGTTCAGGA TGGACAGCCT CAGAGTAGAG AGCTTCAGGC CCCCTCTCCT 360
TATCTTCTGC TAACCTCCAT TCTTACTCCT ACCCTTTCAT CTCAGAATTT TCGCTTTGAT 420
GTTTCCCACT TCCTTCCTAT GGTTACTTTA ACCGAAGTGA GTCAGGTCTT ACTGAAAAAC 480
TGACCACAGC CTGTCCGCTC CCAGCCTTCC CCAGACCAGG GCTGCCCAGG CAGAGCGTGA 540
GGGGGACTAG TGTTTACTCA GCTCATTTTT TTCCTCCTCT CTCCTCTAAG TCACGGGGCT 600
TTGAGTAGGG CTTCCCCAGC CACCGTGCCC CTCCCAGCAG ACCGCAGTCA GAAGCCAATC 660
TCACATTTGT CTGGTGGCTC AGAGAGGGGA CAGAAAGAGC AGCAGCTTAT GTCCTTGGCT 720
ATCCTCTCAA GTGGGCTAAT TTGCTTATTT TCAACTCTGT TGGGTCCAGC CCTGTTGCCT 780
CTGATCTCAG CTCAAAGAGG ATTTGGCGGG AGTTTTTGGT TGTGATAACC AATAACAACC 840
AACTATACGC ACTGCGAACA TCTCCTAGTG CCAGAAGCCC TGTTAGCTCA TTATCTTAAT 900
CCTCAGGATA ACCCAGGCAA TTTGTATTCA CCCTAAAAAC TTCCCCTGGC CGGGTGTGGT 960
GGCTCACGCC TGTAATCCCA GCAATTTGGG AGACTGAGGC AGGCGGATCA CTTGAGGCCA 1020
GGAGTTCCTA ACCAGCCTGG CCAACATGGT GAAACCCCAT CTGTACTAAA AATGCAAAAA 1080
ATTAGCCGGG CGTGGTGGCA CATGCCTGTA GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA 1140
GAATCACTTG AACCTGGGAG GCGGAGGTTG CAGTGAGCTG AGATCATGCC ATTGCACTCC 1200
AGCCTGGAGA CAGGGCGAGA CTCCGTCTCG AAAAGCAACA ACAAAAACAA AAACAACCTC 1260
CAAAAAACCT TCCCCTGTTT ACCTTTCTAA 1290
|
