| Tag | Content |
|---|
EnhancerAtlas ID | HS018-02533 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr10:14747040-14748460 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr10:14747716-14747730 | GAAAAGGGGAAGTT | + | 6.82 | | TBX21 | MA0690.1 | chr10:14747443-14747453 | AAGGTGTGAA | + | 6.02 | | TEAD1 | MA0090.2 | chr10:14747510-14747520 | ATGGAATGTG | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr10 | 14747800 | 14748095 | | chr10 | 14747620 | 14748173 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I014705 | chr10 | 14747542 | 14748127 |
|
Enhancer Sequence | AATAGACAAA GGACTTGAAT AAACATTTCT CCAAAGAAGA TACACAAATG CCAATAAGCT 60
CATGGATTGC TGCACCACAT CACTAATCAT TAGGGAAATG TAAATCAAAA CCACAATGAG 120
ATACGACTTT CACACCCATT AGAATGACCA CTATTTAAAA AAAAGAAAAT AATAAGCAGT 180
GATGAGAATG TAGAGAAACT GGAACCCTTG TACACTGCTG GGGGAACTGT AATGGTGCAG 240
GTGCTATAGA AAACAGTACT CATTCCTAAA AAATAATTAC ACATACAACT ACCCTATGAG 300
CCAGCAATTA GACTTCTGCA TATTGACCCA AAAGAATTAA AAGCAGAGTC TAGAATGGAT 360
ATTTGCACAC CCATGCTCCT AGCAGCATTG TCTACAATAG CCAAAGGTGT GAACAACCCA 420
AATTTTCCCT GATAGAAAAA TGGATAAACA AAGTGTGGTC TAGCCATACA ATGGAATGTG 480
ATTCAGCTTG AAAAAGGAAG GGAATTCTGA CACACACCAC AACATAACTG GATCTTGAAG 540
ACATTATAAT CAAAGAAATA AGCTAGCCAC AGAAAGACAA ATACTATATA TGGTTCCACT 600
CCTACAAGGT CCCTAGAGTA GTCAAATGCA TAGAGAGAAC AAGCAGAATG ATGGTTGCCA 660
AGGGCTAGGT GGAGAAGAAA AGGGGAAGTT GTTTAGTGGG TACAGAGATT CAGTTTTTTG 720
CAAGACGAAA GAGTTCTGGA GATGGAGGGT GGTGATGACT GCACAACAAT GTAAACGTAT 780
TTGATGCCAC TTGTGATCTG AGAGGCCAAA ACAGATGCCC TTTTGTCAAC TAAGAGAAAC 840
TCTAACGTTA AGGCAACAGA AGTTACCTAC AGATCAAGGT TTCAGGACCC AACCGGCAGG 900
GCAAATTTCT AAATTCCTAT GGCTTACAAG AAAAACCGCA CTCTTGCTAA ACTCCTATAC 960
AATAGGAGCT ATCAGGCAAA TTAACATACC CTTCCTAATT CTGATTTACA ACCCAGACCA 1020
CTACAACTCT GTTGAACAGA GGATTGGCCT GATAAACATT CTTTCCTGAT AAGCAACTGC 1080
AGACCTTAAG CCAGTTTCAG CAGCTCATGG AGGCTGTGCA CAAACTGTCT TTGTGTCCTA 1140
TGCTTAACCT TTTGATATAT ACCACCTTGT TCTATTTTAT TTTAAGAGAC AGGGTCTCAC 1200
TCTGTCACCC AGGTGGGAGT ACCGTGGTGC AATCATAACT CATTGCAGCC TCAAACTCCA 1260
AATTGTTTTT TTTTTAAGAC AGCTAAAGTA TCCCTCTTGC CTCAGCCCCC CAAGTAGCTG 1320
GCACTACCAG AACACACCAC CATGCCTGGC TAATTTTAAA TTTTTTTGTA GAGATAAGGT 1380
CCCACTATGT TGCCCAGGCT GGTCTTGAAC TCCTGGCCTC 1420
|
