| Tag | Content |
|---|
EnhancerAtlas ID | HS143-00960 |
Organism | Homo sapiens |
Tissue/cell | NGP |
Coordinate | chr13:110358280-110360940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr13:110359471-110359485 | ACTCCCCAGGGACA | + | 6.05 |
|
| | 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 |
| GH13I109704 | chr13 | 110356439 | 110360251 |
|
Enhancer Sequence | AAAAAAAAAA AAAATTCTCC CAGACATGCT CAGAGCCAAA GCAAGCAAAA TGAGGGTCCT 60
CCACTGAGTG ATTCTCCTGC ACCCTCCTTA GCTGTCCACC AACACTGCCT CCAGTTGTCC 120
CAAGCCTGAA ATGCACTTGA GAACACGTCC TCAAATCCAG TGGAAAAGTC TACATTATTT 180
TGGGAGAACA GAGCATCAGA CAGAGCTCCC AACCCCACCG CTTCCTGTCC TTTGCCTTGA 240
GGACCTCCCT CAGGGTAGGG GGGCCTGTGG GCCAGGAGTG GGCAGCCCAG CCCCTTCGAT 300
TTCACAACTG CCTGGTTTCC TCTCTGGTGG AAATGCACAG GTGGTGACAA AACTGGATGA 360
ATTTCATCTT CTTTACTCTT GTTTTAGAGC TGTGAGTTCG AGTCAGTTAC GGTGTGTGAC 420
TTACTAACCC ATGTTTGCAT CTGTGTGCTT CTGATCTTCA CACACGCTGA GCACATTAGG 480
GGCGCCTTCC TGTGGACCGG GCCCCACACT GGCAATGGGG CAGGCGCACA GTTCCTCCAA 540
AGAACCTCAC AGCTGTGCCT TGTCCTCTGA GAAAAGGTGT CAGCCAGTTC CACTGGACAG 600
CCGGCACTGT CAGAAATCCT ACCTTAGCAG CTGGACCAAG GTCTCACCGG AGAAGATGTG 660
TCAATTCAAT TTCAAGGTCC TTTTATACAA TTTAATCAAA GGTCATCATT AGAAAAAAAA 720
ATCATGATTA AGAAACGAAT AAAATTCAAG TCATACTGTT ACCTCTGTTT TAAACAAAAC 780
AATGTTTCTT TACATATAAA TTTTTATTTC AAAACATTTG ATCCCAGGAA AGTCTTTCAC 840
AATAAGTGAG TTTTTAGCAG ACCAGGAGAG TCATCAGTGG ATAAGAGTTC TGGGGTGAAG 900
GTTTTCACAA AGTGCCCTAG ATTGTTGATG ATATTTTAAT CATCTATCCT TGGAATACAA 960
TGGACATAAA ATCAAGAAGT GTACTGAACC TTGAATGAAA CAGCAGAATG AACTCTGAGT 1020
CCCAGAAAAC ACCTAAGAAC TAAGAATGCG TTTTTAATGC TCATGAAAAA CAAATGGCAA 1080
TATAGAATGT GGGACTAAAG AATGGTTACT TGAAGCCAGA AGTGGGTGTT CTGCAGGTGA 1140
AACCCAAGCG CGGCCCCTCC CCAAGGCTCC TTTCTGTGTT GTGAGTGCCC CACTCCCCAG 1200
GGACAGCACT TTGTTTTCTT TCAGCTTTTC TGACATCATA TGATGCAACC TGATGCAAAG 1260
CAAAGCGATA GGCATCTTGT CACAGGAGAA ATTCACAGAG AGGAGGGGGG CACGCTGCAG 1320
CTGGTGCGGA AATTCTCAAG AGAGGCCTGG GAGTGGAGCT GAGCCGTTGC AGAGGAAGGT 1380
GGAGAACCTC TTGAGAAGTT CATGGACACA TAGCGTGGTT CAGAAGAAAA GTCAGGTTCC 1440
AGTGATTGAA GAAAAAAGCG AGACATTATT GCAGGCAAGG ATCTCCATGT TGGGATACAA 1500
AGGCAATGCT GATTTCAGGA TATCTGTGTA CGTCTGTGTG TCATGGGAAG GGAGGCTGCA 1560
GTTGGACACG AATAGAACAT CTGCTCAGGA CGAGGACACG TGGGATCACA TCCTCAGAGC 1620
CCCGTCGTCT TCAGAGCCCT TCTCTAGGCT GGAGGCAGTG AGGACAGGAT GGGAGTGTCT 1680
CCTCCCTTCC CTGTTTCCCA GGGAGCATGG CCAGCTTGGT GACTGTCACA GCAGGTGAGC 1740
AGCAAACTCC CAGGCCAGCA GGGAGGGGCG ACTGTGAGCA GAATGACAGC CACATGGTAG 1800
GTGTGTACTT TAGAGCAGGG GCCTCTCCTC GAGGTTACCC CAGCTCATGC CCCAGCAGAT 1860
AGCTTGGTGG GAGTGCTGTG CCTGACCCTC CCATAACCTA CGGAGCCCAG GTGGGGAGAG 1920
TCACTCTCCA GATCTTACAT AAAAGATGTA GCACCTCACA CACTGCTGTT ACAGAGCAGA 1980
TAATAAATAT TCATGATATG CAATTGAATA GTTATTTAAA ATGTTTATCT ATGGATGAAT 2040
GAATGAACTG AACAAAGAGC AAAATATACA GACAAGTAAG GTGTCACAAA GCTGGCTCTG 2100
AGTAACCAGC CTGTTATCAA ATTCATTTGT ACAGTAATAA AAGAAAACAT ATCCCACCAG 2160
CCATGTGCCA GGCACTGACA TGGGAGCTTC ACACATATGA AGGCGCAGAG CAATCGGCAC 2220
AATCCTCTGC TTCATGGAAG AGGAAACAAA AGCCCCAAGA GGCTGGGCCG GGAGCCTGAG 2280
GCCCAGCGGG GCCAGCTTCG GGCCACCTCA CTGTGTTTCA AGGCCCGCCG TCCATCACTG 2340
CGGCTGTCAC AATCCCTGTC TTTTCTTGGT TGTCATATTT GCTTCTCACC TCATCATGTC 2400
TATTTTCCAT GTGGTTCAAG CTTTTAGGTT ACATGGCTAA TAGGTTAACC CAAATAAACC 2460
ACATTATGGC TTGTTTATTG CTCTCTGTAC AGCACTACTA AGACGGGTGT TAAACCCAAC 2520
TTCCTCCTCG TGAAAGAACA CCTAAGCCTG GAAACTTCCC ACTTCGCTGT TCATTATAAG 2580
GTTCGAAAAA CACAAACTCC ATGACAGTGC TTCAGAGGTG CTTTCCAGCA GCTCTAGGCA 2640
CAAGGAGTAC TATCATTTGA 2660
|
