| Tag | Content |
|---|
EnhancerAtlas ID | HS182-21974 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:124895070-124897250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr9:124897187-124897199 | GCTGACGTCACC | + | 6.14 | | CREB1 | MA0018.3 | chr9:124897187-124897199 | GCTGACGTCACC | - | 6.14 | | REST | MA0138.2 | chr9:124895586-124895607 | GGTACTGTCCATGGCACTGCT | - | 6.18 |
|
| | 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 |
| GH09I122133 | chr9 | 124896041 | 124896190 | | GH09I122134 | chr9 | 124897141 | 124897290 |
|
Enhancer Sequence | TTGCCCAATA CCATGGCACA GACCTCTCCC ACAGACAGAT GGGCCTGGCT TCACGCATGC 60
TCTTGGAGAG ACTGGAAATA GAAGTGTCGT TGTTCTCCCA GCTCCACCAG GGCTTGAGTT 120
TCTTCACCAT GATGCTGCAG TGTCTATTTC TCCATCTCTC TCCAGTCCTT GGGAAAGTCA 180
CCCCTAGCGA GGGAAAAGGC ACCACGTTTG CCACTAGCCT CGGGCCCCTT TCATGCCCAT 240
GGTTCCATCT AATCCTCACA ACCACTCTGC AAAGTAGACC TTACTTCCTG CATTTCATGG 300
GTGAGGAAAT GAAGGCTCAG AGAATTGGAG TGACTTGCTC AAGGTCACAC AGCTAATAAA 360
TAAGTGGCCG AGCTGGGAAT TGAACCCAGG TCCCTCCGAT CCCAGATGCC AGTAGAAAGA 420
CCATTCTTGA TTTCTGCTTT ACCTAATTGC CTGGTGCCCC TCTCAGTGAC AGCTCTGCTA 480
CCTGGAACTC CTCTCTCTCC TCTTTCTGGG ACCCCAGGTA CTGTCCATGG CACTGCTTCC 540
TCCTTATCCA GGCAGGAAAG GTGCTTAGAC TCAGAAGTAC AGAGGCAAAG AGCCCTTCGA 600
GAGGACTCAG ACCAGTCCCA CTTGACCAGC TCTGCCTCCA GACAGATGAG GAAACTGAGG 660
CCAGGCTTGA GACCTAGAAT TAAAGGTGCA ATCTCCTATC CAACCATGAG GCATGGTGGA 720
AGGTGAATCT CACCCAACAG GATTCTAGGA GGCAGAGCCT CTCAGAAACA GGGGAATCAG 780
TGGAGAACGC ATCAGGGGAT GCGTTCTATG GCAGGCAGGT CTGCTGGTCA GGGCTTGAAG 840
TTTTGGAATG GACTGGCAGA GAGGAGAGGG AACAGGCCAG ATCTGAGGGT GGGGGTTGGG 900
TGGCTTGGCT GAGCTGAAGG GTCAGGCAGC CTTGGCCAGG CTCCCATCTC CAGCCCCAGG 960
GCGAGCGCGT GAGGTGGAGC TGCGACATTC AAGCAGCTTC CTCCCCTTTG TTGGGAGTGA 1020
TGTCGCCCAT TTCCTGGATG TCCAAGAACC GGCTTCAAAC AATAGCGCTG TCAGGAAGCC 1080
AGGAAGGGGC TGGTGCCCTG CGCCTGGTCC TACCCCATCC CTCCCCACCT CCTGAGACCC 1140
GGCCAGGCCA TCCTTTATGC TTATCTCTTT GAGTCTGATG CCTCTGCCAC CAGCCAGCTG 1200
TGTTTCTGCG GGCAGGCCAC CTAACTTCTC TGGGCCTGAG CTCTCCATCT AAAACTTGGG 1260
GAACAGATTC TTACCTAGCA GAGCTGGCAC ATCGATCAAA GGAGGTGATA ACAGTAGTAG 1320
GGCTGGTGGC CAACACACCA CACGTAGATA ACTCACGTGG AAACGCTTGG CACGTGGTAG 1380
GCTTGAAAAA TGTGATTTGA CAGTTTTCAT GATTCAGAGT CAATTCACCT TTTCCAAATG 1440
CCTACTAAGT GTCAAGCATT TCCGCATGTG TTATCTCCGT ATGGTAGGTT AAGACTTACG 1500
GTTTTGGAAT CAGACAAAAC TGGGTTTAAA TCCCAGTTCT ACCACTTACT ATATATAGCT 1560
GTGTGACCCG CGATAATGAG ATAACCTTTC CGAGCATCAG CTTCTTCATC CATAAAACGG 1620
GAATAACAGG AACGCCTATT TCATGAAGTC ATCGTGAGAA ATATGTGGGC CAATAAATGT 1680
AGAAAACTTG GTGCAGTGCT CGGCAAACAG CAAGTACCTA ATAAGCGTCA GTAATTATCA 1740
TTTCCACCAT GGCCTTCTAC AGGCCTATTT CATATCTTTG CTTACACAGC TCCCCTGCCT 1800
CTGAGCCCAT CCTCTCTAAA AGTTGTGCAG GCATCCAACT CTGCACAACT TTTAATATTG 1860
AGTTGCAGCC ACACAGGTAG TCCACAGTGA GGGAGTCAGA AGTCTAGGCT CAATCCTAAT 1920
TTCACTACTA TCTGAACCCT TCCGATCTTT GGGCCTCCGT TTCCCCATCT GTGAAGTAAA 1980
GGGAATTTAT GGTTCTCTGG GGGTCTCACA ATTCCGACAC TCCATGAGTT AGTTCAGTCC 2040
TCTGACACCG GACCATTCCT GACACTGGAC TTGGCAATGG GTCAGAGCCC TCACCCGGCA 2100
CGAGAGGGCG ACTGCCTGCT GACGTCACCA GCAGGCTGGA ATCCTCCCCA AATGCGGAGA 2160
GCTGCACAAC GGGTTCAAGC 2180
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