| Tag | Content |
|---|
EnhancerAtlas ID | HS108-21452 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:10379240-10381850 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr2:10379799-10379809 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr2:10379799-10379809 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr2:10379799-10379809 | ATTTTCCATT | + | 6.02 | | NR2C2 | MA0504.1 | chr2:10380478-10380493 | GTGGGTCAGAGGGCA | + | 6.01 | | ZNF263 | MA0528.1 | chr2:10379800-10379821 | TTTTCCATTTCGCCCTCCTCC | - | 6.74 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCTCAGCGGC AGCCCCTTCC TACCCCCCCG GCTTGCAGAG GAGGGTCCAG GGCTGTGCTT 60
GGGTCCTGAG TCCTGGAGTC AGGCAAGGCA GGGCTCCCAG GTGGGCCCTG CATCTAGGCT 120
TTGGGGCCAG GTCTCTCTAG AGCCCACCCA TCATGGGGGG AGCTGGCCGG TGGGACATCT 180
GGGTCCCCAA AAGGAGCTGT CCTCTTTGGT TGGTTCCCAT AAAGTCCCTT CCTCCACACT 240
CCCAGCTCTG TGCAGGGTCT TCAGGATGCA CGGGCAGCAG AGGGGCCTCC TTGGGTCCCT 300
CCAGAGGCTG GCCGTGCTGG CCGGGCTGGC CGGGGTGGAG GCACCCGCCC CCGTAGGCTT 360
CCATCCCACT CCCACCCCAG GGTCCGCAGG CAGCGTGTCC ACACCTACTT AATTCTCTTT 420
TAAATGGAAG GGAAAAAATA GCAAAGAAGA GTCCCAGGTG CTCTAAAAGG CTTTCACAGG 480
CTCCGAGCAA TTAGGAGGCT GGGCTGCGGG AAGCGCTGAG TGCTGGGAGG TTACTCAGGG 540
AGGCAAAGTC ACGTGCAGAA TTTTCCATTT CGCCCTCCTC CAATAACAGC CTGTCCATGT 600
GAGGGACACG GGGGAGTTCA CACTGCCCTC CCTGATGGTG TCCGGGGGCA TGCAGGCAAT 660
GGCCCCTCCC GAAAGGAGAA GCACCAGCAC TGCCTGTCCT TGGGAGCCCT TCGGGGCTTC 720
TTTCTAGTTC CTTCAACCCC TACTGCGTGT GCTGCCCCTG CTGGCGAGGC CGGCCCCCAG 780
CGCAGACAGG GCCTCATCGG TAGCTGCACT CAGGGTGCTG TTGGGGAGGA AGGCACCAGC 840
ACTGTACACC TTAGCCCAGC CCAGAGTCAT AGGCCCTCCT ATGTGCAAGA CCCCAGGGAA 900
GCACAGGGCT TCAGAGGGGC TTAGTGTGGT CCCCCTTACG ATCCTGGACT TTCATGGGGG 960
AATGGTTAGA AGGAGGCAGA GAGCCCACTC TTGAGGAGTA CCTCCCACAA GATGCCCTTT 1020
GCCTCTTCCG CAATAGCCTC ACAGTGCAGG GTCTCAGCCT GCGGACAGCT CAAGGGACCT 1080
GGCGGTGCTG GGCCTGGCTG AGAACAACAC ACGCTACATG GACCCACATG CACCCCACTC 1140
ACACCCCCAC GAGAACCACC TAGTACCTGC AGCTGCACCG GGCCAGAGGC CCAGGGTCCT 1200
CTGCAGGTGT CTTCACTTCC CTGAGCCTCC GCATCCTCGT GGGTCAGAGG GCAGAAGCCT 1260
GGGGACCTCT GCAGGCATCT TAACTTCCCT GAGCCTCCGT ATCCTTGTGG GTCGAACAAG 1320
GCCAGCCACA TTGACCTCCC TGGGAAGTGC CATCCTCCTA GGCGTGTCCC CAGAGGCCGG 1380
CCTAGCACAG AAGGGTCTGG AAAGGGCGGC TGCTGCCATC ACACGCGCAC AGCACACACG 1440
CACGTACACA TTAACAACCC TACCTCAGGG AAGCAGAGGG CTGAGCCGAG GGTCTGCAGG 1500
GAAGCCTTGG GAGGGAGGAA ACTGAGGCAA GCACGGGGCC TGGGTCAACA TCTCCAGGTG 1560
GAAGGGGGTG AGGCTGAGGG CTTGGGGGGA CTGGGTGCAG GGTGGGAGGG GGCTGCTGGA 1620
GAGAGGGGGT TTCACAGTCC TGCCCTCCCC ACAGAGGAGC TGCGTGGGTA GGCTGAAGCT 1680
GTGCCACCTC AGGCCTTCCT CTTAGCCTAC TCCCGCTTGC CTGTCCCTGT CCCCTGAGCT 1740
ATCCTAGAGC ACCCACCCTC CTATGGTGTC CAAGCGACTA GAATCAGACC TGAAAGAAGG 1800
AGGTTCCTTC AGGCAATGTT TGAGGAAAGA CCAGCCGGGG CCGGCATAGA AGATGCTTTT 1860
GCCCTAACCC TAGCCCTGAC CCTTCCTGCG GGGAGCTCAG CCCTTCGGCC CTGCCCGCTG 1920
GCCCCCTAGG CCACCCTCTT GGGTCCCAGG CCTGGGAGCA TGTGACCTGC ATCCCGGGGA 1980
ACCCAGGACT GTCCTTCCCC TGCAGGCCCA GGGGAAGGGC CCTGCACCCA GCATGGGGTG 2040
AGGGGTGGCA ACAAACCTCT CTAGAGGGAG ACCCAGAGCT TCCTCCTTTC AGCCATGGCT 2100
CCCATAATCA AAAGCCCCAG CCCATGGCCA CAGCCAGCAT TACCCAGAGC CCAGACGCAG 2160
AGATTAATCG GCAGGAGCAA ACACCGCCAG CCCCGTGGCA CACGGCAAAC AGAAGGGGTG 2220
AGGCCCGGCC TGGGGGCCGT GGGCAGAGGC CACCGGGGTA TGGCTTCAGT CAGCAGGCCC 2280
CAGCAGGCTG GCCACGGCCA CTAAAGGTGC CGCAAAACAA GACTGGGAGG AGTAGCGTGG 2340
AGCTTTGGTG CTTGGAGTGA TTCATCCTCA CACCCACCGG GGGCAGGGCT CACAGAGGGG 2400
CTGGGGGTGG GGAGCCTGGA CTGTCCACTT CATGAAACGG GTGCTCTCAA AACTCCCCCT 2460
CCCTTGGCCA AACTTCCGCC CCCAGCCCCT GCCTCGCCGC ATCCTTTCAA GCAGCCTCTT 2520
CTTTTTGGCC CAGGGATTTT TGTAAACCAG GTCAACCAAA GGCACTTCGA ACTCAACCTT 2580
GCATTTCTAA TAATACTCAG ATTCATGGGC 2610
|
