| Tag | Content |
|---|
EnhancerAtlas ID | HS182-11559 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:47853930-47855360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr19:47854412-47854433 | TCTCATTTTCTTTTTCTTTTT | + | 6.02 | | ZNF263 | MA0528.1 | chr19:47854199-47854220 | GATGGAGGGGACAGAGGGGGA | + | 6.02 | | ZNF263 | MA0528.1 | chr19:47854764-47854785 | TCTTCCTCTCCCTCTTTCACC | - | 6.06 | | ZNF263 | MA0528.1 | chr19:47854761-47854782 | TTCTCTTCCTCTCCCTCTTTC | - | 6.61 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 47854917 | 47855115 | | chr19 | 47854648 | 47855360 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I047351 | chr19 | 47854901 | 47855457 |
|
Enhancer Sequence | CCTCCCAAAG TGCTGGGATT ATAGGCGTGA GCCACCATGC CCGGCCTGAA AAAGCATTTT 60
TTTTTTAATG AGAAAGATGG AGAAAGTCAA ATGGAGAACT GAAGAGAGAT GGAGAAAGGA 120
AGAGTTGGAT TACAGAGAAA AATCAGACTA CAGAATGACT CATAAGTGAA GAGAGATGCG 180
AGCTGACTAG GACAGGGAAG AGAGATGAGG GTGATGATGA ACAAGACGGA CTGAAAAAGA 240
GACAGAGGCC TGAAGATGGA GTGGAGAGAG ATGGAGGGGA CAGAGGGGGA AACAAACCCA 300
CTGAAGGCCA TGAGCCCAGG GCAAATAGGC CAAGAGACCA AAAGATGGTC AGAGACACAG 360
TTATACAGAA ACTAGAAGAT GCAGACAATC TAGAAGCCAA AAAAGATAGA TACCTTGAGA 420
GGAGCGGGAT GCTGTCAGTG GGGCCCAGCA TGCATAAGCA GTTTCTAGCC TCAGAAGAAT 480
GCTCTCATTT TCTTTTTCTT TTTTTTTTTT TTTTTTTTTT TTTGAGACAG AGTCTCGCTC 540
TGTTGCCCAG GCTGGAGTGC AGTGGCTCAG TCTTGGCTTC CTGCAAGCTC TGCCTCCAGG 600
GTTCGAGTGA TTCTCCTGCC TCAGCCTCCC GAGTCGCTGG GACTACCCGA GTAGCCAGGT 660
GCCCGCCACC ACACCTGGCT AATTTTTTTT CTCCAGCCTG GGTGACAGAG CAAGACTCCA 720
TCTCAAAACA AAAAAGACTC CAACTGTAAG CAAAAAGGCA TTTTCTGGTG TAGCTGAGAA 780
GTGGGGGGTT GAAGGGAACT AAGCTTCAAG ACCTAAATGA TGTTGCCAAG CTTCTCTTCC 840
TCTCCCTCTT TCACCTCTCC CTGTGGTGCA GTGACCATTC TTGTGCCTGT ATCTAGTTAT 900
TTCTCTAGGA TAGATTTTAG GAAAGACTCT GTCATGTTCC AGAGCTACCA CAAAGAGCTC 960
CAGGCTTATA TCAAACTTGC CTGATTATGA TGGATAAAAT GAGAGCTTTT CTGTCCTAGC 1020
AACCGAGTGT AAATTCCACA AAAGGGCCCT GATTGGCCCT TCTTGGATCA TGTGTCCGCT 1080
TCTCAGGCCA ATCCTTGGTT AGAGGGGGAG TAGACTACTA AGACTGGCCA GGTCTTTGTT 1140
ACTTGCCTAC CCAATAGGGG TTCTTTGTCT TAAAGGCCCT CAGAACCATG TAGAATCGAG 1200
GAAGGGCTGT TGTCCAAAGG AAGGTGGATA CTGTCCTCAG AAAAGAAGTA AAGGGTTGTG 1260
CCAGGCAGGC AAAAATTACA TATAACACTT GCAAAATTTT GCCTTTTATC TCAATGTTCT 1320
GAATCTCACT GGACCCCGGG TGAAGAACCC TTGCCTTATT CTTTTCATTA TATCACACCT 1380
CTCTCCTATT ACTGCCTGTG GAGACAAGGT TCTGCTGTTG GTTGGCCATG 1430
|
