| Tag | Content |
|---|
EnhancerAtlas ID | HS140-00207 |
Organism | Homo sapiens |
Tissue/cell | Namalwa |
Coordinate | chr1:149781940-149783430 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr1:149782649-149782660 | AAGAGGATTAA | + | 6.14 | | EWSR1-FLI1 | MA0149.1 | chr1:149783191-149783209 | GCCTCCTTCCCTCCATCC | - | 6.3 | | EWSR1-FLI1 | MA0149.1 | chr1:149783195-149783213 | CCTTCCCTCCATCCCTCC | - | 6.57 | | ZNF263 | MA0528.1 | chr1:149783191-149783212 | GCCTCCTTCCCTCCATCCCTC | - | 6.12 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGGAAAAAAA AAATCATGTA TACCGCATTT TATATCTTTT AATTGGGTGT AAATTTGAAT 60
TTCAACATCA TAAAAATTAG TAAAATTCAT TTTAAGCACA AAGTTGTTAA TTCCCCCAAG 120
ATTTATCAAG AATGGCTTAA TTTCAAAGGC TGTCAAGTTA ATTATAAGCT AAGATTTTCC 180
AGTTGCACCA AGGGTATATT TTATTTGGCA AAAGAAACAT CCACTGGCTT TTGTCAGGAT 240
GAGTCTTGAG TTATTCAAGT TTTGAACTGA GAGGTCTTCA GAAATTCACC CCACATATTA 300
ACTGTGGCCT TCTCTACACC ACAAATTCCC CTCCACTCAT CCTCAAATTG TTTCCTTTCT 360
CAGGACATCT GTGACACAAA GACTGTGACA CACCCACAGG TCGATTAACA TGAGGACCCA 420
ACACCTATTA AAACATCCAC ACTCCTGAGA ACACTAAAAA CCAACCACCT CGTCAGGTCC 480
CACCTCCAGT CTAGCTGAAT CAGGAAACCT CAGGAGAAGC ACCTGGAAGC AGGTTTAACA 540
AGCGCAAAGG TGACTCTTAT AATTGGGAAA GTTTGGAACC AAGACAGGGT TCTTGTCCTG 600
GAGGAAGTAT TTTCCTGTGG AGAAGGACCT GTAAACAGCC TATGAAGTGC TCAGCTTTCA 660
CCAAGAAAAG AAAAACATGG GCTGATAGGG TTAAGGAAAC GTTTGACTGA AGAGGATTAA 720
ATCCTGAAGG TTAGGGATGT CTTTGGGCGC TGGGGTCTCT CAATCACCAA AGATCGACAT 780
TACAGGCCAG GTAGCTCTTT GTCCCCCCAG AGGACTGTCC TGTGCCTTAT GCTTAGCACT 840
CCTGGCCTCT GCCCATTGGA TACTTCTAGC ACCTCCCCCG CAACACACAC ACACCTGACA 900
ACCCAAAACA TCTACAGATA TTGCCAAATA CTCCACAGGG GGTGGGGTGG TGGCAATATA 960
TCTCCCTGTT TGAAGTCACT GGAATGGAAG TTAGGGGAGG ATGGCTAAGT CAGGACTTGC 1020
AAAAAGGCTA AGGGACGAAA GCACATGGCT ATATTAGACA AAGTTTGTGA CAGACGCCTG 1080
TAGGTATATG GTAAGGAAAA CAGATTAAAA CACTAAGAAA TAGTAAGAGG TCGGACCGAG 1140
GGTTTCTCAT CTGTATGGGA AATCTCATCT CGTTCATTAC TTTCAGAAAC AAAAAGGAAA 1200
ACGACTTTAA AGATACAGGT TAAAGGCCGA AGGGGTGTAG AACCACCCCC CGCCTCCTTC 1260
CCTCCATCCC TCCCAAATAT CCCAGAACGA GTCAAACCTT TCGAATCTCG TAGCACAGAT 1320
AACAAGCAAC TCAGTAAGAC TGGACGGGGA TGACTGAGGG CCAACTCATT ACAGGACTAC 1380
AGGAAACTCC TTAGTCCTAA ACCCGAATGC ATCCGTGACC ATGGTAACAC TCCCTACCTG 1440
ACCAAAAGCT ATCAAACGCT CTGACAAGTG TTTACAGCTG CTTTCTCGAT 1490
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