| Tag | Content |
|---|
EnhancerAtlas ID | HS138-25666 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr22:41703210-41705100 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr22:41704155-41704166 | TCTGATTGGTT | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr22 | 41704034 | 41704989 | | chr22 | 41703267 | 41703573 | | chr22 | 41703800 | 41705024 | | chr22 | 41703703 | 41703900 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I041307 | chr22 | 41703170 | 41705141 |
|
Enhancer Sequence | ACCTCGTGAT CCACCCGCCT TGGCCTCCCT ACTGCTGGGA TTATAGGCAT GAGCCCGTGC 60
TGGGCCTGAA GTCGGCTCCT TTCATCACAT TTCATGGCCC CTGGAAAACA AGCTCATTTT 120
CCTTCCTCTG TCAGCACCAG CTACAGATTC CTTCTCACCA AATTCATTCC CCCCAGGGAG 180
ACTGTTTCTT TGCAGGCATG TTGGTTGTGT TGGTGCCGTG TTGGTTGTGT TGGTGCTGTC 240
TCCCCACCGG GCTATGGAGG CCCAGAGGGA GGGACATTCC TGCATTCAGA GCGCTTGTTC 300
CCTTCAGAAA CATCTGGTAA CTTCAGTTCT GCAGCATCAC AGCTCCTCAG CGTCAGAGGC 360
TGAGACACAA GCTTGGTGGG GATCGTGGGG ATACGATCAC CCATATAGCA GCACATAACA 420
CCCATATAAC AGCAGCCCCC ATATGGTTAA CACCACTGTA TACCAGCATC GTGCTTGACA 480
TTTCCTATGC CTTCTCTTAT TGAATCCACT TAACAGCTCT TCAAGACCAG AGCAATCATT 540
GGCAGCCCCA TCTTGTAGAT GAGGAGCCTG AGGCTCAGAA AGACTAAGTT AACACTTCTG 600
AGATCACACA GCTGAGGTAG AGAAGGGAGT CAGATGAAGC CACCTGGCAT CCGAGGTCTT 660
AGCTGCCATG CAGGAGACAG TCTTCAGGTT ACTTCCAGTT TCCTCGAAGC TCTTTTCTTA 720
TCAATCTGGA AATCCTAACT ACCACCAACA TTTGTGTCCT GCTGTGTCCA CAGTCTCTCA 780
TTAATTGTCA TGACAGTCTT TTGAGGTAAG GTAAGAGGTG TCCCTGTTTT TCAGAAGAAA 840
AAGACTGAGG CATCATCACC CACCCACTGC TCTTCCTACC CAGTCCACAA TGTGACTTGG 900
GAGGGGAACA GGGTATTGGA TTCCCTGAGA CCGAGAACCA TGTCTTCTGA TTGGTTTGTG 960
TTACTGAAGT GCTGGAGTCA GCTGATGATC ATTCCTTGAG CACTTCCTGT GAGGGCTGCA 1020
GGGAAGGTGG GGGCTCTGGC CCTCCTGGGG TTTTTAGAGG TCGCCCTGGT TCAGCTATGC 1080
TCTTGTTCCC TGGAGCATCT CTGTGTCATC CCTCTCCCTC CACAGGCTGA GGAACGCAGG 1140
GCAGGGAGCC CAAAGTCCTG AGTTTCATTC CCAACTCCTG TTCATGCTGG CTGTATGATG 1200
GAGGCATTAT TATTTTGTCA TTCTTGGCTT CTGTCTCCTT TTCTGTGAAA CGGCCGTACT 1260
GATCCTGTCG AATCTGCATC AGGGGTTGTA GTTATGATCA TTTAATAGCC TTCAGAATAT 1320
TCCTGAATCT TCTTCACTGT CTGCCTTGAT CCAGGCCTGA ACCACTGCAG TAGCCTCCTA 1380
ACCAATCTCC CAGTATCCTC TCTTGTCATA CGTCCTCCCT GCAGTAGCCA AAAGGATCTT 1440
CTTGCGAAAT AAATAAGCTC CTGTCACTCT TCTGCTGAAA ACTCTCCTGC AGTTTCCTGA 1500
CACACGCAAA ACACAGCCCT GGCTCCCGGC ATGGCCTGTG AGTGGTTCTG AGACCAGCCT 1560
CGCCTGCCCC TTGCACTTTG CCTCCCACGT GGCTTGCCCT TGCTTGGGTG TTGCAGCCAC 1620
GGTGGCCTTC TGAGTTTTCC TGGAACATTA TCAGCTTGTT CCCACCTCAG GGCCATTGCC 1680
TGTGCCCTGT CCCCTGCTAG GTAGGTGCCC TCTTACCCCA CCTCCTATCT TCCATGGCTG 1740
GCTACCTATC TCTCTTAAAT GTCAGCTTCC TCCTAAGGGC CTTCCCTAAA CTCCCAGTCT 1800
GCTTTTTTTT TTTTTTTTTT TTTGAGACGG AGTTTCGCTC TGTCGCCCAG GCTGGAGTGC 1860
AGTGGCGCGA TCTCGACTCA CTGCAAGCTC 1890
|
