| Tag | Content |
|---|
EnhancerAtlas ID | HS182-00115 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:8341940-8343360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr1:8343165-8343176 | GTTTTATTGGT | - | 6.32 | | NFAT5 | MA0606.1 | chr1:8342559-8342569 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr1:8342559-8342569 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr1:8342559-8342569 | AATGGAAAAT | - | 6.02 | | SP4 | MA0685.1 | chr1:8342656-8342673 | GGAGGGGGAGTGGCTTG | - | 6.17 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I008281 | chr1 | 8341891 | 8342660 | | GH01I008283 | chr1 | 8343081 | 8344197 |
|
Enhancer Sequence | ATCAGATGAC GGTGACTTAG ACAAGACAGA AGGTTTATTT TTCCTGCACA TAAAAGCCCA 60
AGCAGACATT AGGTGGGGCT GTGGGGTGAG TGGCTCTGTT GTGTGAGGTC AGCCTGCAGC 120
CCGCCTCCTC CACGTGGCTC TGCTGCGCCC AGGGTGCTGT CTTCCTCTGC ATGGTCAAAG 180
GCAGTGCACT TGCTCATGTC CATGCTGCAG TCCTCAGAAA GGGAAAGGGG TCAAGGACAA 240
GCAGTGTCTT TTCAGAAGCG TCCTGGGAGC TCAGGTCCAC ACTGGCCAGT GTGGGACCTC 300
TCACACTGGC CAGTGAGAGA GGCTGGCCTT GTAGTCACCA GTGCGTGGCC AGTCAAACCC 360
AGGGGGCTTC AATTCCAAAA GAAAAAAGGG AACTGGATGA CAGGGAACCA GCAGCAGTGG 420
CTGCCACAGA CAGCTCTGCC GAGCTGGGAG GAAGCTGGAG GAGCGGAGCG GGCAGAGGGG 480
CAGAGGGAGT GGTCAAGAGA GACGCTGAGG TCCCAACAGT AAGAGATTGT ACTAGAGGGA 540
GATCTCAGAG AAGGTGGGCA CTGTAGGGCA CAGACGGAGA CCTTGGCCTT GGACAGGACG 600
AAGGCGGGAA GCAGGAAAGA ATGGAAAATA GCAGGAGGTT TGCAGGTCTG GCAGCCACCA 660
GTAACAGCCA TTTTCTGTGT AAGATAGGAA TCCGAGTCTT CTGCTGTGAT TGAGTGGGAG 720
GGGGAGTGGC TTGGTGTCTG AGAAGGGGGA CAGTTTGAAA CAGTCCTTGC TAAGAGGGGT 780
GATCAGGAAC CTACTTGCTG GTGGTGGGAC GCCACCCTGG GAATCTCACC AAAGCTTGGC 840
AGGATTGAGG GGCAGGTGAA GTTGGTTACC ATGGTATATC ATAGCCCTGA CCTTGGGGGC 900
TGGAAGATTT CAGTTAGGGA TGCAAAGCAA TTCAAGTAAA AGTTTTGAGA AAGTAGACAA 960
CTGAGTTTCT CCAAAGTCCC TATGAGGACA GAAATGAGGA TGCTTTCACT GGAGCGATGA 1020
CACAATTATT TCAGTAAGTC TCCCAGAGTG CGGTAGAAGA AAACGCTTTG TGTTTGCAAT 1080
AATAGATCTG GGGAAAAGGA CTGATGAGAA CCAACATTTC CATGAAGTCA CACTGACATT 1140
TTTTATTCGT TAGACTTTGT CAACCAACGC ATGCACTTTT CTGAACAGCA AGCATCATTC 1200
ACGAATGCAG AACAAAAACA GATAGGTTTT ATTGGTTTCA GAAAGACATG GCGAGATGAG 1260
CAGCAGGCAG CTTGCTCGTT CCATGCAGTG GAGGAGGAAG AGGCTGGGCC CCTGCTGTGT 1320
GGGGGCAGCC CGGGAAGGAC ATGGTCACCA GCCTTGGGTC ATCAGTAATT AGTGAGCGTC 1380
ACGGGTAAAG AGTTTTATAG TCAGTAATAG TTTTCTGTAA 1420
|
