| Tag | Content |
|---|
EnhancerAtlas ID | HS112-04435 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr13:110358320-110360840 |
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 | GCAAGCAAAA TGAGGGTCCT CCACTGAGTG ATTCTCCTGC ACCCTCCTTA GCTGTCCACC 60
AACACTGCCT CCAGTTGTCC CAAGCCTGAA ATGCACTTGA GAACACGTCC TCAAATCCAG 120
TGGAAAAGTC TACATTATTT TGGGAGAACA GAGCATCAGA CAGAGCTCCC AACCCCACCG 180
CTTCCTGTCC TTTGCCTTGA GGACCTCCCT CAGGGTAGGG GGGCCTGTGG GCCAGGAGTG 240
GGCAGCCCAG CCCCTTCGAT TTCACAACTG CCTGGTTTCC TCTCTGGTGG AAATGCACAG 300
GTGGTGACAA AACTGGATGA ATTTCATCTT CTTTACTCTT GTTTTAGAGC TGTGAGTTCG 360
AGTCAGTTAC GGTGTGTGAC TTACTAACCC ATGTTTGCAT CTGTGTGCTT CTGATCTTCA 420
CACACGCTGA GCACATTAGG GGCGCCTTCC TGTGGACCGG GCCCCACACT GGCAATGGGG 480
CAGGCGCACA GTTCCTCCAA AGAACCTCAC AGCTGTGCCT TGTCCTCTGA GAAAAGGTGT 540
CAGCCAGTTC CACTGGACAG CCGGCACTGT CAGAAATCCT ACCTTAGCAG CTGGACCAAG 600
GTCTCACCGG AGAAGATGTG TCAATTCAAT TTCAAGGTCC TTTTATACAA TTTAATCAAA 660
GGTCATCATT AGAAAAAAAA ATCATGATTA AGAAACGAAT AAAATTCAAG TCATACTGTT 720
ACCTCTGTTT TAAACAAAAC AATGTTTCTT TACATATAAA TTTTTATTTC AAAACATTTG 780
ATCCCAGGAA AGTCTTTCAC AATAAGTGAG TTTTTAGCAG ACCAGGAGAG TCATCAGTGG 840
ATAAGAGTTC TGGGGTGAAG GTTTTCACAA AGTGCCCTAG ATTGTTGATG ATATTTTAAT 900
CATCTATCCT TGGAATACAA TGGACATAAA ATCAAGAAGT GTACTGAACC TTGAATGAAA 960
CAGCAGAATG AACTCTGAGT CCCAGAAAAC ACCTAAGAAC TAAGAATGCG TTTTTAATGC 1020
TCATGAAAAA CAAATGGCAA TATAGAATGT GGGACTAAAG AATGGTTACT TGAAGCCAGA 1080
AGTGGGTGTT CTGCAGGTGA AACCCAAGCG CGGCCCCTCC CCAAGGCTCC TTTCTGTGTT 1140
GTGAGTGCCC CACTCCCCAG GGACAGCACT TTGTTTTCTT TCAGCTTTTC TGACATCATA 1200
TGATGCAACC TGATGCAAAG CAAAGCGATA GGCATCTTGT CACAGGAGAA ATTCACAGAG 1260
AGGAGGGGGG CACGCTGCAG CTGGTGCGGA AATTCTCAAG AGAGGCCTGG GAGTGGAGCT 1320
GAGCCGTTGC AGAGGAAGGT GGAGAACCTC TTGAGAAGTT CATGGACACA TAGCGTGGTT 1380
CAGAAGAAAA GTCAGGTTCC AGTGATTGAA GAAAAAAGCG AGACATTATT GCAGGCAAGG 1440
ATCTCCATGT TGGGATACAA AGGCAATGCT GATTTCAGGA TATCTGTGTA CGTCTGTGTG 1500
TCATGGGAAG GGAGGCTGCA GTTGGACACG AATAGAACAT CTGCTCAGGA CGAGGACACG 1560
TGGGATCACA TCCTCAGAGC CCCGTCGTCT TCAGAGCCCT TCTCTAGGCT GGAGGCAGTG 1620
AGGACAGGAT GGGAGTGTCT CCTCCCTTCC CTGTTTCCCA GGGAGCATGG CCAGCTTGGT 1680
GACTGTCACA GCAGGTGAGC AGCAAACTCC CAGGCCAGCA GGGAGGGGCG ACTGTGAGCA 1740
GAATGACAGC CACATGGTAG GTGTGTACTT TAGAGCAGGG GCCTCTCCTC GAGGTTACCC 1800
CAGCTCATGC CCCAGCAGAT AGCTTGGTGG GAGTGCTGTG CCTGACCCTC CCATAACCTA 1860
CGGAGCCCAG GTGGGGAGAG TCACTCTCCA GATCTTACAT AAAAGATGTA GCACCTCACA 1920
CACTGCTGTT ACAGAGCAGA TAATAAATAT TCATGATATG CAATTGAATA GTTATTTAAA 1980
ATGTTTATCT ATGGATGAAT GAATGAACTG AACAAAGAGC AAAATATACA GACAAGTAAG 2040
GTGTCACAAA GCTGGCTCTG AGTAACCAGC CTGTTATCAA ATTCATTTGT ACAGTAATAA 2100
AAGAAAACAT ATCCCACCAG CCATGTGCCA GGCACTGACA TGGGAGCTTC ACACATATGA 2160
AGGCGCAGAG CAATCGGCAC AATCCTCTGC TTCATGGAAG AGGAAACAAA AGCCCCAAGA 2220
GGCTGGGCCG GGAGCCTGAG GCCCAGCGGG GCCAGCTTCG GGCCACCTCA CTGTGTTTCA 2280
AGGCCCGCCG TCCATCACTG CGGCTGTCAC AATCCCTGTC TTTTCTTGGT TGTCATATTT 2340
GCTTCTCACC TCATCATGTC TATTTTCCAT GTGGTTCAAG CTTTTAGGTT ACATGGCTAA 2400
TAGGTTAACC CAAATAAACC ACATTATGGC TTGTTTATTG CTCTCTGTAC AGCACTACTA 2460
AGACGGGTGT TAAACCCAAC TTCCTCCTCG TGAAAGAACA CCTAAGCCTG GAAACTTCCC 2520
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