| Tag | Content |
|---|
EnhancerAtlas ID | HS098-22831 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:89698820-89700940 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr16:89699049-89699060 | ACAGATAAGGA | - | 6.14 | | ZNF263 | MA0528.1 | chr16:89699356-89699377 | GCAGGAGGAGGAGGGAGGGGA | + | 6.15 | | ZNF263 | MA0528.1 | chr16:89699362-89699383 | GGAGGAGGGAGGGGAGAGCAG | + | 6.49 | | ZNF263 | MA0528.1 | chr16:89699359-89699380 | GGAGGAGGAGGGAGGGGAGAG | + | 9.53 | | Zfx | MA0146.2 | chr16:89700376-89700390 | CAGGCCTCAGCCCC | - | 6.21 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr16 | 89699468 | 89700263 | | chr16 | 89700794 | 89700938 | | chr16 | 89698855 | 89699182 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I089631 | chr16 | 89697242 | 89700208 |
|
Enhancer Sequence | CGACACAGGG GCAGGAAGTA TCTTCAACCC AAATGGCTGT GTGCCCGCTA AAAACGGGGG 60
GTTTTAAAGT CACAAAGGAA AAGGAGGAGA ATGGATCCCG GGGGCAGCCA GCAGTCTCCC 120
CACGAACAGC TGCCTGAGTG TGTGCTTGCC GCTTTTCCAG CACTTTCCAG CACTCCTTGG 180
AGCAGGACGC CGGCTTCCAT ATCCCAGCTA AGGGCATTGC CCCAGCTGCA CAGATAAGGA 240
GGGTGGGTCT GATTAGCAGA ACTGCCATTT GCCCTGGCCA TGAGGCAGGC AGGGCCTCCC 300
TCCCACTGAG AAACCAGAGG CCCCACCTTC CCATCGTTTT CTCCAGCAAG AGTGGAGAGG 360
GCTGGCGGGG CACAGTGGCT CACAGGTGTG GTCCCAGCAC TTTGGGAGAC CGAGGTGGGA 420
GGACTGCTTG AACCCAGAAG GTTGGGGGCT GCAGTGAGCT GTGATTGCAC CCCTGCCCTC 480
CAGCCTGGGC AACAGAGTGA GACCCTGTCT CAAAAAGAAA AAAGAAAGGA GGGGCTGCAG 540
GAGGAGGAGG GAGGGGAGAG CAGAGAGCTG CCCCATTGCA GCCTGTCCCT CCAAGGGCGG 600
CTCCTGGGGT CCTAGGAATC CCTACCCATC CCAGGCTAAT GTCTGAGATG GGCCGCCTGC 660
GTCCTCAGGC CAAGGAGTAA AGTCTCCTGG GAGCCCTGCC CAGCCCCACC CAGGACAGTG 720
CCCAGTGTAG GGTTGCACCT AGCGATGAGG CTGCTGCCCG GGCAGGGTCC CTGGCTGGAG 780
CTCATGGTTC CCTCAGCAAG TGCGTCCTGA CCACCCACTC TGCTCCGAGG GCTGGGGAGA 840
GGCCCGTGCC AGCCCAGGCT GTCATGTGGA CTCGCTGTGG CCAGGGACAA CCTCGCTGAC 900
GCAGGAGCTT TGGGAGAGAC TCACACCAGC ATCAGGCGTG CGCCCGCCCA TCTGCCCAGG 960
GGTGGGGCCG GAAAGCGTGC CAGGCTGGGC TTGGGGGCAC TAGCCCAGGG GAGGTCAGGA 1020
ACGACTGGGA CCCAGGAAGG GCAGAGCCCT CCCCTTCTTT CCCCTGAGGA GCTCCATGGG 1080
TGCATTCGCC TTGGAAAAGC TCATTGCGGG CACATAGATT TGAGCTGGGT CACAGAAAGC 1140
AGAGCCCGCA GCTGGAAATG ATTAACAGTT ACTCATCTGC CTCTCCCAGC TGCCCTCCAA 1200
GGAAAGCACC AAGACACCCT CATGTTACAG ATGGGGAAAC TGAGACACAG AGGGAGCTGT 1260
CCTCAAGGAG AGCACCAAAA CACCCTCATG TTACAGATGG GGAAACTGAG ACACAGAGGG 1320
AGCTGTCCTC CAAGGAAGGC ACCAAGACAC CCTCATGTTA CAGATGGGGA AACTGAGGCA 1380
CAGGGATGGG TCTGGAAACT GCAAGTGGAG GGGCCCCTGT GGCCTCATCC CAGCGCACAC 1440
CCTCACAAGG CAGTCCCCCC GAGACAGGGG CACAGCCCAC ATTACAGGAA GGAGACTGAG 1500
GCCCCAGACC CAGTGACGGG GAAGGGGAAC CCTGGGCATT CCCCAGGGTC GGGGGTCAGG 1560
CCTCAGCCCC TTCCCATCCT CCTCACAGCC TGGTTGAAAC ACAGATGAGA TCGTAGCCTA 1620
GAGCCTGCCC TGGGCCCCTT AGAGCTGCAT TTCTATTTTT CTTTTCTCTT CTCTTCTTCT 1680
TTTTTTTTTT TTTTTGGAGG GAGTCTCGCT CTGTCGCCCA GGCTGGAGTG CAGTGGTGCG 1740
ATCTCGGCTC ACTGCAAGCT CTGCCTCCTG GGTTCCTGCC ATTGTCCTGC CTCAGCCTCT 1800
TGAGTAGCTG GGACTACAGG CACCCGCCAC CACTCCCGGC TAATTTTTGT ATTTTTAGTA 1860
GAGACGGGGT TTCACCATGT TAGCCAGGAT GATCTCGATC TCCTGACCTT GTGATCTGCC 1920
CACCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACCCTGCCT GGCCTGAGAA 1980
TTGCATTCCT AACGACAGTG GATTCCCTTT GCTCCTGGTC TCTGCCAGGC CCTGTTGGGC 2040
AGCTGGATTC GGACCCTCTG GGATCCTCAC TCAGCCACCA GCTCTGACAG CCCCAGCTCC 2100
CCCTTCCTCT GCGTTCCCCT 2120
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