| Tag | Content |
|---|
EnhancerAtlas ID | HS197-00632 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr1:41233580-41235020 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr1:41233933-41233943 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr1:41233933-41233943 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr1:41233933-41233943 | ATTTTCCATT | + | 6.02 | | POU4F2 | MA0683.1 | chr1:41234312-41234328 | GTCATTATATATGCAG | - | 6.05 | | ZNF263 | MA0528.1 | chr1:41234425-41234446 | CCTCCCCTTTTCTCCTCCCCT | - | 6.41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGGTTGCAG TGAGCTGAGA TTGTGCCACT GCACTCCAGC CTGGGCGACA GAGTGAGACT 60
CTGTCTCAAA AAATAAAAAT TAAAAAAAGT CCGTTTTGGG AACAGAACTA AAGCCAAAAA 120
ATGGGAGAGG CTGGGGAGAA GCAAGAAAGT GGTAGCTGAA GGCAATGAAA ATCTTTGTAA 180
CAACAGGTTG TAATTATGAC AACCTAATAC TTAGTAGGTG CTCAGTAAAT GTTTGTTGAA 240
TGAAGCTGAA TGAATAATAT GTAAATAAAA TGTAAAGGTA AATGAAATCT CAGCTAATAT 300
GAATGGCAAT CCTGCTGGCC ACAGAGCAGT TAACCTTCTT ATCTATGTGG AATATTTTCC 360
ATTTGTCTCA GGCTCACTTG TTTATTCTGC AACATTTCTG GAATACTAAC TTTGTATGGG 420
CTCCTGCCCT CAGGCATCTT ATAGGCTGTT GGAAGGAAAA GGACCAAAAT AAGGAACAAT 480
AGTAAAAAAT AGTCATGAAG CCTGTCATAC CTGTTCCCTT TCTTGTTCCT CATAGCCTCA 540
TGGGTAGGCC TGCAGGGGTT GTTTTTGGCC ATGGTGAGGA CATTTGAGAG GACAGTCCTT 600
GTCTTGCAGG CTGGCTGTGA TGATTCCAGG AAATGGTACA CAGAGGACAC TGCTGGCCAA 660
ATGTTCCATA GGAACACATG TGCATGCACA CCGCAGTCTT CTTTCTAGTT TACCGAGCTG 720
CTCCCAGCAG TTGTCATTAT ATATGCAGTT CTACATGTCA GTACATTTAT CTAAAATCCA 780
TTCACAGTCC ACACATAAGA TTTTAAGTAC TTGTGATAAA TGTTGTCTTT GTTCCACTCC 840
CGGTCCCTCC CCTTTTCTCC TCCCCTCCTT TGGCCCAGAG GGCTGCACAG TGCCTCTCTC 900
GGAAAAAGTA CTTCATAGGT TTGCCATGAG GACTGCTGGG ACCAAGGCCA CTTGCTCGCC 960
AGGGTGTTTC ATATTCCAGT CAGATGATCT GGGTGATACG GGTTTGGTTT GGAGCCCACC 1020
TTCCAAGAAT GAAAGAGGCC ACTTACCACT TTGTCTGACA CTTTGCAGTC CGCCTTCACT 1080
GGCTGAAAGA CTGACTCTTA GGACTTCTAC CCCAAACCAT AGCACCTAGG GTCCATGTGT 1140
TCTGTTTGAG CCTCAGAGTT TGAGATGAGT GGGTGGTTGA GGGAGTAGGC ATTCATTAGA 1200
GAGATGGGTG TGGGAACTAT CTATTATGTG CTCCAGGATT CTCGATGTCA CTTTGTGCTG 1260
CCAACTCTTG ACGTAGCCAT CAGTGCTAGA TTAGGAGGGG TGCTTGCTTG CTTACTACCC 1320
ATTGAGCACC TGCTGGGCAC TTTATATGCA TTGTCTCATT TGATCTTTAT GACCCTCTTT 1380
TGGGTGGTGG GCTGGTGGAT CAGACCCTGC AGCTGACATA CCAACTCTAC CATCTTGATT 1440
|
