| Tag | Content |
|---|
EnhancerAtlas ID | HS052-22000 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr2:198575720-198576830 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr2:198575780-198575791 | GAGAGGATTAG | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AATATATGTT ATTTCAGCAC AACAAAACTC ACCCTGCCCC TTCCTCTTGC AGGAAGTTTG 60
GAGAGGATTA GTTAACTCTT ATCAAGAGGA ACACACCAAA TTTGGAGGTT AACAACAGTT 120
AACAACCAAG TTAATTAAGG TTAATGGGAA TTTTAACCTT TTAGGAAGAG TATCTTATTC 180
TTTCTGGAGA CAGGACAGGA GAAGCCCTGG TTAAACTTCC TTCCTATGTC ACCAATAACT 240
ACTTTGAGCA GAGGGGAAGG GACTAACCAA TTTAGAGGTG AAATTAGCTG CTTCTCTTTA 300
GTAGGTAGTC TTGGGTTACC CAGAATAGAT CCTCTGAATT AAAGGAACTA CCTAGCAGGA 360
AACAGTTGGC CATATTTAAA TAGTTTGTTT AGGATTGTAT CACATTAGTT TCCACTTTTC 420
ATGATGAGGG AAGGGAACTA GAAGGAACTA CACACCAACA GGATCTTCCT ATGGCCCCGA 480
CAACTAGAAA TAATATATCC TCTACCATGC CTCTTCTGAT GAGTACCACT TGGGAGGTTC 540
AGCCATACTT GGATGTTCAC CAAGGTAAGC AAGGCATAGT ACATATGTTT CATCCTTGGC 600
CTTGAGCTGA ATTGTACCCC CTTAGCTAAT GGCACAGTTT ACTCACCATG GATTTTAAAG 660
TCCACTGCTC CTCACTTAAG AACAGGATGG TGTGAGATGT TCAAGATGTT TCAGGAAACC 720
AAGTGTGCCA TCTGCAAGAA GAAAATTATA GCTCCAAGGA GGGATGAGCC CTGCCCTTGA 780
GTCACTTCTG GATGAAACAT CTGCAGAGGG CCTGACTCAC TGGGTAAGCT GAAGGGACAG 840
ACCCAGGAAT AACTATGGAA ATGGAGGATG CCTTTCTTAG ATTATGATGT GGGAGAAATG 900
GTACTAACAC CTCTGTGCTA CTGCTATTAA GGCCATGCCT TGTACATGTA CCCTCATTAG 960
TTGAGAATCA ATTGTTTATG GGATTTAACA TGATGATGAA GCTTCAAAAA CTAGATAATG 1020
ATTGTTATAG GTTGGTATCA TCATATTATT CTTTTAATAC ATTCCATAAA AATATGACCA 1080
ATTACACATT TTTTCCTGAT TGTATATTTT 1110
|
| |
|
|
|
