| Tag | Content |
|---|
EnhancerAtlas ID | HS018-01464 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr1:157087050-157088150 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:157087168-157087183 | TGACCTCTGCCCCCT | - | 7.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCCCTCCCTG CCATCATCTG TTTGTGCTGC TCTTTGAGGG AACCTGGGAA AAAACAGAAG 60
GCAGGCTTAA TGACTCTCTG TAACAGAGGG TCCCTCCCCT GCAGCCAGAA TCTGGTGCTG 120
ACCTCTGCCC CCTGGAGAGA GGGGTCCTTC CATCCTCCTC TCCCTGGTGA TACCCTGCAG 180
GACTCCAGGT GAGAGGCCAG TGGCTTCCCC CCTCACTGGC CCTTAGCTCT TTGGGACCCA 240
GGTTGTAAGG CTTGGACTGT CTCCTAGACC AGGCTTTGGG CTGAAGGTGG GATGGAGTCG 300
ACAACCTGAT AGAACTGAGA CAAGCTAGAA AGGCCTGCTG CTGCTGGGTC CCAGACTTTC 360
ACTTCCTGTT TTGGCTGCCT CTGCAGGGCT TATGGCCCAC TCCCCATTGT CTCTAGACCA 420
GATCCCAGAT ACTAGAGCCA GGGGTCTGGA GACAGTGAGG GGGACCCCCT CATCCCCAAT 480
TCCTCCCCAC CTCTGTATCA ACCCGGGCCC AGCCTCCACT GTCAGTCATG GGGGAGTCAG 540
GTGGGCTGAC CTGCATTCTG GGAAGGCTTT CTCCTTCCTT TTTCAGTCCC CCTGGAGCCT 600
GTTTGGCCAG AGCTGAAGGG CCCCTCCCCT GGGCCTGCTC ACAGGTGCTT GTTCCCCCTC 660
CTGCTGTGTT CTTGCCAGGG TCTCAACACT CCAGGCTGGG ACACGTGGCC TGACACCTGG 720
AGAAACACTT AAGGTTGGGC CTTCCCCCTC CTCTTCCTAT TCTGCATGTC TGATTCTTAG 780
ACGCTGCTTA GAACTGTCTT CACCCTCGCC TCAGAGATAC AAGGCAATGG GGAAAGTATG 840
TGATCTGGAG TCAGGAGACC TCGGTTTGAA TCATTAGGAT AAGCCACCTG CTCCGGGCCT 900
CACTTGTCTC ATCTGTCAGA CAGGGATGGT GGTACCAAAA AAAGCCAATG TGAAGGCACA 960
AAGCCGCAGG AGGGTAAAAT AACCATGATG ATGGGATGGG ACCTCACTTA AACATTGTGG 1020
TCACTTCACT AAATGCTTTA TGTGCATCAT TTAATCCTTG AAACAGCCCT AAAACATAGG 1080
GAAACTGAGG CACGGAGAGG 1100
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