| Tag | Content |
|---|
EnhancerAtlas ID | HS018-01570 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr1:161186400-161187770 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr1:161187349-161187360 | TTCTGTGGTTT | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGAGACCTGA GCGTCAGCTG AGAAATAGAG GCAGAAATGG GAAGGTCTCT GAAGCTCTAC 60
AGCTCCAGCC ACTATCTAAG AATTCTCACT CCTCGTTCAC TCTGTGTTGT CTGTGCTGGA 120
TTGGTGTGTG TGTGTTGGTG GCAGCTGGGT GTTGGGGAGG AGGAGGTCAG TAAACTTCAG 180
GGAAACTGTG GAAATTGAAA GAGAATGACT GGGGAGGAAT TCCAGCAGCC TAGCTGAGAA 240
GGTGGGAGCA AGTATTAAGT TAGCCACTGG TCTGCTGCCG TGGGATGAGG AGGGAGGAGG 300
CCCGCTGAGG CACAAAGGAA AGCATGGGCT TTAGAGGCAG AAAACCTGCA TTTGAGTTCC 360
AGCTCTGTCA CTTAACTCTG TGGCTCTGAG TGAGTTACTT AGCTTTTCCG AGCCTTGGTT 420
TCGTCACCCA TAAAATGGCG ATGATGATGT TTCCCTCACA GGGTAGTTTT AAGATTTGTG 480
CAATATCGTG TGTGTGAAAG AGTGTTGCAG AATAAAAAGT ACTTGACCGA TGTCAGCAAT 540
TGACTGACGT TAGTCACATG TTCCCTACTG GTCCTCTGAT ACGGGGTGAG AGCAGTCTCT 600
GGAGCCCAGA CTTGATTTGA TTTTTTAAAT TGCACAAAAC TTCCCCTCTC AGAGACCCAG 660
AGAGTGAGTA ATAGGGCAGA GTAACAGGAG CTGGAATCCA TATAGCTGTG GTCATTCCCC 720
CAGCCTTGTG TTCAGGGCCA AAGGTATCTG TAAGGTCTGG GAAAAACAGA CACACTTTTT 780
TTTTTTTTTT TTTTTTTTAC ATATTTAAGT GTCTTGTGGT GGGACAGAAA GCAACAAGGC 840
TGAGGCTAGG AGATGACCAA TGATAGAGTA ATTGCCTTCT CTCCCTTCCC CAGCTCACAT 900
CCTTCCTGTC CAGCCCTCAG CCACAGGTCA CAGGACTTAG TAGAGACACT TCTGTGGTTT 960
CTTCACTGAA ATTTGCCACT ACCTCTCCCT CCCACTACCC ATCTTGGCTG AGGTTTTGGT 1020
TTCAGTCCAG TGGACTCAGA TGGGTCCCTT GAGGTGGATA AAGTGCTCAA TGGTGCCTGA 1080
AGAACCCACA GTGCTAAAAA GAAAAGGTTG GGGGCTGAGG GGGAAGGCCT CAATTATTAG 1140
TCCGTGTGAG TCCCATTTCA ATAGAACCCT CAAGCTTCCT ATCCTAGCCT GACCCTATGG 1200
TGTGGGAGGA GGGAAAGGTA AGGGCAGTGG AAGGCCAGAG AGAAACAGAA TTTCTTCCCT 1260
TAGACGGCTC CCCTCCAGGC CCTGTCCTAC CTCCCAGAGC CCCTTCCCTT CTCTCCTCTG 1320
AGTACCAGAT CCTCCCTGAT ACCCCCGACC CCATGGGCAT CCTCTATCCC 1370
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