Tag | Content |
---|
EnhancerAtlas ID | HS073-09891 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr22:39728200-39729670 |
Target genes | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr22:39728597-39728618 | AGCCTGTTTCACTTTCTTATC | + | 6.07 |
|
| 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 |
GH22I039331 | chr22 | 39727993 | 39729667 |
|
Enhancer Sequence | TAGGGTCTAG GGCCTTGCGC TGGGTTAGTC TTTGTCTTTT TTTTTTTTTT GAGACAGAGT 60 CTCGCTCTGT CACCCAGGCT GGAGTGCAAT GACTCGCTAC AACCTCTGCC TCCCGGGTTC 120 AAGCAATTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGATT ACAGGCACCT ACCACTACAC 180 CTGGCTAATT TTTTGTATTT TTAGTAGAGA TGGGGTTTTG CCATGTTGGC CAGGCTGGTC 240 TCAAACTCCT GACCTCAGGT GATCCTCCCG TCTCGGCCTC CCAAAGTGCT GGGATTAGAG 300 GTGTGAGCCA CCACGCCTGG CCTAGTCTTT GGTTTAAGAG AATGTTGTGG CTGGTTTGAT 360 CTTCTATCCA GACCCAACTT TCTCCATATC AGCAATAAGC CTGTTTCACT TTCTTATCAT 420 TCATGTACTC ATTAGAGTGG CACTTTTAAT TTCCTTTGAA AGCTTTTCCT TTGCATTCAC 480 AACTTGGCTA ACTGCATAGT GGAAGAGGCC TAGTTTTCAG CGTATCTCAG TTTTTGACAT 540 GCCTTCCTCA TTAAGCCTAA TCATTTCCAG CTTTTGATTT AAAGCAAGAG ACATGTGACA 600 CTTCCTTTCA CTTGAACACT GAGAGGCCAT TGTAGGGTTA TTAACTGGCC TAAATCCAGC 660 CTGTCTCGGC TGTTGGCATG CCTTCCTCAC TAAGCTTAAT CATTGCTAGT TTTTGATTGA 720 AACTGAGAGA CAGGACTCTT CCTTTCACTT GAACACTTAG AGGCCATTGA GCAGTTATCA 780 GCTGGCCTAA TTTCAGTACT GTTGTATCTC AAAAAATAGG GCTGCCCTAG AGAGGGAAAG 840 AGACAGAGAA ATGGTGAGTC AATAGAAGAG TCAGAACACA CACATTTATC AATTAAATTC 900 ACCATCTCGG GCCGGGGGCA GTGGCTCACG CCTGTAATCC CAGGACTTTG GGAGGCCGAG 960 GTGGGGGGAT CACGAGGTGA GGAGATCGAG ACCATCCTGG CTAACACGGT GAAACCCCGT 1020 CTCTACTAAA AATACAAAAA AATTAGCCGG GCGTGGTGGT GGGCACCTGT AGTCCCAGCT 1080 ACTCAGGAGG CTGAGGCAGG AGAATGGCAT GAACCCGGGG GGCAGAGCTT GCAGTGAGCC 1140 GAGATCGTGC CACTGCACTC CAGCCTGGGT GACAGAGTGA GACTCTGTCT CAAAAAAAAA 1200 AAAAAAAAGA TGGCCTGAGA CTCCTTCCAC GTATTTACCT TTTAGAATTC TGATGGGCCA 1260 TGTTTCTTTT TCTTCCTTTT TTTTTTTTTG AGACAGAGTC TTGTTCCATC TCCCAAGTTG 1320 TAGTACAGTG GCATGATCTC AGCTCACTGA AACCTCTGCC TCTCCCCAGT TCAAGAGATT 1380 CTCCAGCCTC AGCCTCCTGA ATAGCTGGGA TTACAGGCGC ACGCCACCAC ACCCAGCTAA 1440 TTTTTGTAAT TTTTTAGTAG AGAAGGGGTT 1470
|