| Tag | Content |
|---|
EnhancerAtlas ID | HS141-16655 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr7:12261870-12263070 |
Target genes | |
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 | chr7:12262592-12262602 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr7:12262592-12262602 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr7:12262592-12262602 | AATGGAAAAT | - | 6.02 | | SPI1 | MA0080.4 | chr7:12262750-12262764 | GAAAAGAGGAAGTT | + | 7.14 | | SPIC | MA0687.1 | chr7:12262750-12262764 | GAAAAGAGGAAGTT | + | 6.31 |
|
| | 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 |
| GH07I012222 | chr7 | 12262237 | 12262790 |
|
Enhancer Sequence | TTGGTTGCTA TCACTAGAGC CATAAGAAAA ATCATTACTA GTTAATTTTG TAATGGAGAC 60
ATATATTTTG TCAGTAAACT AGCCAACTTT TCAATTTGGA ATGAAATACT AGATGGAATG 120
TTGTTTTATT GTCCCACCAG GTTCAGTAAT GTTCGTTATG GCTACAAACG TGGTATACAG 180
AGTAATTTAG AACATGATTC ATTTATTCAC AACTAGGACT GACTTATAAG CCCTAAGGAC 240
TAGATTATGA TGGATTCACC CGCCCATAAG TAATTAAAAA TAAAACGCTG AAGTGTAGAA 300
AATCCAACAA AGTTCAGATT TTATTATGAT GATGTTAAAC ACTTCTTATG CCTTTTTATG 360
TATTTTGGTG TGTTATAGAT ACTATAAACG TGTTTAAATT TCCTATTAGG TAATCCAGTG 420
GGGATCACTA CCCCTACTCA GGTTGAGAGA GTCCAAAATG AGTGAGTGGG AACTGTTTTG 480
ATTGCTCAAG ACAACAGCAT GGACTTAGTA GCAGTGACTT AGCAAATTTG TGTTTGCTTG 540
TATTATTTTG TTTTTTAATA AACCAGTTTG CTCTGTTCTT AACTTGGGCA ACTTAAAACA 600
CTAAGAAATA TTTATAAAAT ATCTGCAGGA GGCACTTTAA TTGCTCTTGT AATACATACA 660
AAGATTAAAT CCATCAGAGC ATTTAGAAAG GAAATGGTGG CGGAGAGTGG AAGAAACAAT 720
AAAATGGAAA ATTTTTGTAT AAGTAGATTG TAAGGAAAAT AAGTAATTGT CATGCAAGAC 780
TCAAAAACAA AAAAAGGATG TTGTGGGCAT CCAATAGAGG ACTTGTATGT TAGAGAGAAC 840
AGGAAATAGT TATTTGAACT CTGGTTTTGA GGTTAACCTT GAAAAGAGGA AGTTTTTACC 900
TACAAATTTT TCCTTGTCTT ATACCTGCAT GAAATATCTT TTCTTGATTA GAAAAAGAAA 960
TGTAACAACA CCTTCAAAGC AGAGTTGATC AATGTAAAAA AAATCTTAAA AACTGAGTAT 1020
GTAAGTACTT TGAGATGAGA ATACTCAAAA AAAGACTAAT TATAGTAAGA ATCATTGATG 1080
AGCCATGTGG TTGTGTCATT TTTTTTTAAT TTTAAAAATA TGGAGGATGT GCAGGTTTGT 1140
TACATAGGTA AATGTGTGCC ATGGTGGTTT ATTGTACCCA TCAACCCATC CCCTAGGTAT 1200
|
