| Tag | Content |
|---|
EnhancerAtlas ID | HS144-00673 |
Organism | Homo sapiens |
Tissue/cell | NH-A |
Coordinate | chr1:145713080-145715060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:145713744-145713763 | TGGCCGCTAGAGGGCGCTG | + | 7.3 | | MSC | MA0665.1 | chr1:145713159-145713169 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr1:145713159-145713169 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr1:145713159-145713169 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr1:145713159-145713169 | AACAGCTGTT | - | 6.02 |
|
| | 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 |
| GH01I145720 | chr1 | 145713284 | 145714909 |
|
Enhancer Sequence | GGACTCTAAC CCAAGTTATG AGAGTCTTTC TCTTGGAGTC CCCTTTGTCC CTCTCCTCAC 60
AGCCGCTCAT CCATTCACGA ACAGCTGTTA ACACAAGAAC GACTGTACTA AGTAATAAGG 120
TCATAAAGTG TCAAGGGGCA GCACAGGAGA AATTCTGGAT GAGGGATGTG GAAAGGCTGC 180
AAGATGGCAA TGAAGTTAGG CCTTCATAGT TGTTTGTGGG CTCTGGGGAG CTGGTGACTA 240
AAGAATACGG TGGGTGAATT AAGGTGGGGA ATGGGCTGAG GAGATCTGGC TTCCAGTCCT 300
GGCTCCGCAC TAGGTAGCTG TGGAATGTTG ACAAGGTCGT GTCCCTTCTC TAGGCGTGTT 360
TCCTAAGGGA CTGGTGCAGC GGGATGGGAG GGGCGCAGGG TAGGGACCGC TTCCAAGGAG 420
AGAGAGGACA GGCGGGAGGG GCTGATGCAG CTGGTCACTC CGCTGGAGTG GCCAGACTTC 480
GCGGTGCCTA GGGCCGAGTT GAAGAAGAGC ATGTAAGTCT GTTGTGGGCC CCTCACCAGC 540
GCTGGGGGGC AGCGAGGTCA CTGGGCAAGG ATGCTCTGGG AAGTGACCTT GGTGCCCGGG 600
AGGGGAGCAC CCTGTTGTGA TGCAGGCGGG GCAGCGCGGA GCCGGCGGCG CTGATTTCGC 660
ACTCTGGCCG CTAGAGGGCG CTGCCTTTCA GCCAAAGCCG AGTGACCCCC TACCTGCCCC 720
GCGTTGGCCC GCGTCACTCC AGCCATGGGC CATCCAGCGA GCATGGGGGC TAGCCAGGGA 780
AAGTCTAAAC TAGGAGGGGA GATGAGGGGG TGCAAAGTTG GGCCTGGTGG GTCCTGGGGA 840
CGCAGCATGT ACTAGAGCGG CACCTGGCCC TCAACAGAGG GGAGAGCGGG TGGTCGTGAG 900
AAGTCTGGGA ATTTTCCGGG CCCACTACAC GCCAGGGGCG GGTCTCCCCT CTTAAAACGT 960
TGTGAGCCCC AGCGCGGGCA GGGGGGAGGG TGCCCGTGGA GTTGGCATCC TCATCTTTGA 1020
TGGTCCCCGG GGCTCCTGAG CTGCGCTGGT GGCCCCAGGG CTCGGTGCCT CTCTCAGGCG 1080
ACAGCTCACA GACGGCGGGA AACTCTTCCC TCCCGCACCT TCGGAGGCGG TCCTGGAGTC 1140
TTGTGGACTC CTGGGTTCAA ATCCAAGCTT TGTGTGACCA GCACATTGCT GGACCTCACT 1200
CAGCCTCACA TTCCTCTTGT GTTTAAAACT ACCTCATAGG AATGTGGTGA CGGTTAGATG 1260
ACACATAAAG CTTTGCCAGA GGTTTTCTGG GGAGGGTGGG GACAAGAGGG CAAGGAAGAG 1320
TCTCCATTTC CTCTGCCACC GGAGCCCGGA TCTAACCTCT CAGAGGAGCT GGAAGGTCAG 1380
CTCTGAGCTC CACAAATACC TCTGTATACA GATCTCCCAC GACACTGAAA AAGATGCCCA 1440
GAAAGATCTC ATTTGCAGCT GTGAAGGGGC TTCTTTTTCA ATCTCCACAA CCCCAACTGC 1500
CTTAAAGTAG AACCAGACTT GTTAGTAGAC AGAGGTTTGG GCTGGGGGGC CCTTGAAGCT 1560
CTTGTCTGAG ATCTCAGGCT TCCTGCTCAA CACACCAAAG CAGGTGCCTG ACATAAAGGC 1620
GCCATGGACC TCTTTGGTGG TCTGGGAAGG CATATGGAGT CCCTTCTCAG AACAACATTT 1680
AAAAATTAAT AAGATACATG GGATAATAAA GGGAACAAAT TATGACAAGA CAGTTGTCAA 1740
AACATTAGAA GAATGTGTGG TAGAGCAGTA CACATGCTTC TTTAGATTTG ACATCAGCCT 1800
AATAACTGTT GTAATTCTGT AGTAGTGCTG AGCGTTAAGG ACATTTGGAG AAATCTATAA 1860
AAACTGTAAT GAGATTTGAA AATATTTGTG TTTTCTATTG ATGGCAAATT CTATTGTGGT 1920
TCATTGTCTA CATTCATAAC TGAAGCAAGT GCTGACTTTC AATTAAAGAT TAGTGAAAAT 1980
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