| Tag | Content |
|---|
EnhancerAtlas ID | HS091-14715 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr15:49152650-49155150 |
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 | chr15:49154199-49154218 | CAACCACCAGATGGTGCTA | + | 6.51 |
|
| | 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 |
| GH15I048861 | chr15 | 49154141 | 49154330 |
|
Enhancer Sequence | CCAAGATGGC GTCATTGCAC TCCAGTCTGG GCGACGAGTG AAACTCCATC TCAAAAATAA 60
AAATAATAAT AATAAATAAA AATAAAAATG AAGTCAAAAT AGAAAGTCAT ATCAAAATGG 120
AAACAACAAT TTTTGCAATT TTATTTTTTC TTAGGATTGA GGAGATGTTG AGAGATGAAG 180
ATGAGGAAGA TAATGAGAGA AGCAGGATAC TTAAGCCTAA ATAAATAAAT AAGAAAAGCT 240
AAATTGTACT TCCAGTGAGG GCGATGAGAG AATAGGATGT TTAAAAGAAC TCCGTGAAAA 300
GATTCAGATC TGAGTTCAAG TTCCAATTAT GCCACTACTT ATGTGACCTT GAACAAGTCA 360
CTTTATGGCA AGGTCCTTGT CTGCCAAGAC AATGTCCTGA GTCATCTTTG AAGTCTTTTT 420
GTTTTACAGA AACCCTATTC TTCCTCTGTC ATGGAAGCTC AAAGTCTCTG AGGAACAGGG 480
CGGCATGTGG GTACACAGAA ATGAATGAAT CAATCAGACA CATCAACCAG CCTCTAACGC 540
TTCTGGCGTA CCTCTAGAAT GTCTTATTTA TCTCAACTTT TCTGATTCTG ATGCTTTGAG 600
GTTTGGGTCC TGTTCATAGG CTGATGCTAT CAACATAATT TTCTGCTTTT CTTTGGATTA 660
GCCTATTACT ACCATATTAC TTTATTTATT ATAGAGACAG GTGTCTCACT ACGTTGCTCA 720
GACTGGACTT GAACTCCTGG GCTCAAGTGA TCCTCCTGCT TCAGCCTCCC AAGTAGCTGG 780
GACTACAGGC ATGCCCCAAC ACACCCAGCT TGAGAAGACT GGACAAAAAT AAAAGAACAA 840
ACAGTGGTGT CTGTCTGTCT CCAGGCAAGA TGCAACAGCA GACAAACAGA CTGACCTCAT 900
GCAGATGTTC TGCCCAGTCT CACCACCTTC AGGGAGCACA TGTACTTTCA CAGTTCCATT 960
GTTGCCTCTC ATAGACATGC TATGTTGCTC TATGGAAATG GTCTTTTTTA GGTTGGTCAT 1020
GGGACAGGAT AGAGGTGGGC CTTGAATCAC ATATAAATAT GCCCATTTCC CAGGATTAAA 1080
ACCAATTCCA AAAGCTTGGC CAAGAATTGC CCAATTTTCA GCTAAAGGGA AAGAAGAAAG 1140
ACAAGTAACT ATATATAAAA AGAGCCAAGT CACAAAAAAG AGGGTGCCTT TTCAGGGATA 1200
TGGTAACTTT GTTACCAAGG CCTGAGCTTT GCTTCCCATG TCTGGAATCA GATGAAAGTC 1260
TGGATTTTTT TCATCCCACC TGTAGCAGGA TGGGCTCACA CTTCCAGCCC TGGGTATCAA 1320
GTACTAAACT AAGATTCAAA AGAACCTGAG ATACATATTC ATCTGTCTTT TTTATTTGGT 1380
TATTGAATTA GGTAGTCATA AACAAGAGGA TTACAACTAT TACTAAAGGA TAACAGACAC 1440
TTCTTTACTA CTTTTATATT TGTTCTTAAT AAACAGTTTT TTTGTTTTGT TTCTGTCTTT 1500
TCCTTTTATA CTTAGAAAAC CAGAAATTCA AAAGTTCAGC TTTTCAGGTC AACCACCAGA 1560
TGGTGCTATG GGATCAAAGC AGGGAGTCCT CCATACTTTA GGAAGAAACA ACCTCAAAGA 1620
GGCAAGCCAG TATTCAGTTC ATAGCTAATT AATACCACCA GGACAGTCGT AGGCATACTT 1680
TATAACTATA AACATAAATA AAAATAAGTG GATTAATTTA AGTTGGTTTT ACTGGTTTTG 1740
GGGTTTTTTT TTTTTTAACT TTCTTCAGAG ACCCAGAAGC ATGGCCTTCC TATATCCAGG 1800
TAGTCCAAGC AGTCCAGTCC TATTCACAGA CTAGATTCAG GGAAAATATT AAAACATTCC 1860
TGGACTGCCA CACATTTGGA GTAAGACAAT GTGGATTTCC TCATTTACAG CAATTACAGA 1920
AGCAGGGTGT ATTAATCACT AACTAAACTC AAAACATTCT TACTGGAACT TAACCTTTTC 1980
TATAAAAAAG GCCTTTGATA AAATGAAGAG TTCACTAAAG GGTCCTAGCC AAGATGGAAA 2040
AAGTGGGAAC TGCCCTGATT TAAATGCACT AATGCTAAAA GCGAATCAAG CAAAAGGAAG 2100
AGTGGGAAGC TTCGGGATTG TCAGCATGAA GCCCAGTCTC CTCTGCTCAT CTCCACTTCC 2160
TGTCAACCAT ACTGTCCTCC TCATCCCTGC AATCTGGCTC CTGCCTTTCT AGGTGTACAA 2220
AAATTGAGCT TTCCAGAGTG ACCAGTGGCC TGTTAATTGC TGGGCGAAAT AGCATCTTCC 2280
CACCCTCATG CCCCTTAACT CCTTTTCAGT GTGTGACCAT CTGAGATGTC TCCTTCAGAA 2340
GAACCTTGCT CTTCCCCTCT GTTAGGTAAT ACTCATTTCT TGACTTCCTC CTGTCCCCTG 2400
ACTACTCCTT AGGCAAGTCA CTGTCTCCTG TGGCTTCCCC CACTCCCTGA CATCCTTAGC 2460
CCTCTTCTTT CTAGGTTCTG CTAAGAAGTT GCAGTTTTTT 2500
|
