| Tag | Content |
|---|
EnhancerAtlas ID | HS056-08890 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chr2:101010240-101011970 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIC | MA0161.2 | chr2:101011876-101011887 | TCTGCCAAGTA | - | 6.62 |
| | | 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 |
| GH02I100393 | chr2 | 101010337 | 101012478 |
| Enhancer Sequence | CAATCTAAGG AAAAAAACGA ACAAGAGGTT AACTTGATGC CACAGGAGGT CACAGCTGAG 60
GGGGCGGGAG AGGGAAGAAT GAGCGGAGTG CAGCACTGTG TATGGGACCC TCACGTGCCG 120
AGGCTGCCAT GAATGCATTC CACACGTCTC TTAATCTACT CCAAGATCCT GTGGATTAAT 180
CCTGTTATTA CCACACTTTG CAGGTGAGAA AACAGAGGCT TGGAAAACCT TACCTGTCCA 240
AGGCCACAGT ACTCATTGTA GGCAGTCACT GTGAAGACAT CTATTTAATC TACCTTCTGT 300
TTTACTTGAA TGATTCAAAA CTTCAAGAAT GTTTACAAAT TTTGTTCCTG GGCAGAAAAT 360
CATAAGGGCA GGAACTCTGA GTCAGGAATA GATGGTGCCA GGGAAAGTTA CTTTAAGGGC 420
ATATTTTTAA AAGTTCAATT CAAATTGCCA GGGGAAGGGG GGCAAGAGAA AACAGAGAGT 480
CAGGCTTCAC GCTCCAGAGG GCAGGAGCAG GTCTGGGTGA GCTGCAAGCG GGCGGCAGCA 540
GAGCATGGCC CTGGGGAGGA GGGCCGGCAG CAGTGACGAT GACAAAGACG ATGACAACAG 600
TGACATCACA GAACACGGTG TGATTACGAC AGGCCAGAAA CTGCTCTCTG TGCTTTGCCG 660
TGTCTTCACT CACTGAGTCT CACAAAAGCC CCATGAGTGC TCAGGGCAAC AGCAGGACAC 720
TCCTCACCAG GAGCATCTCT GGTAAGGGTT GTAAGGATGG GCAGGTGCCA TGCAGGTCAG 780
GCGCCATGCA AGGCAGGTGG CTGCAGACCC AGGAGGCAAA ATCCAGCTGG TGACCTGACG 840
TGAGCCGCTG CTTTTGCATC CTCACTCCTT TTCAGCCTTG CTCTCCTGGG CCACCTGAGA 900
GCTACTACAT GAGAACTTTC TCATCTATTA GCTAAGGACT CCATCTTCTT TTTTTTTTTT 960
TTTGAGACAG AGTCTTGCTC TGTCGCCCCA GCTAGAGTAC GGTGGCCAGA TCTTGGCTCA 1020
CTGCAACCCT TGCCTCCAGG GTTCAAGCGA TTCTCCTGCT TCAGCCTCCT GAGTAGCTAG 1080
GACTACACGT GTGTGCCACC ACAGCGGGCT ATTTTTTTTT TTTTAGTAGA AACGGGGTTT 1140
CTGTCAGTCA CACTTGTCTT GAACTCCTGA CTTCAAATGA TCCGCCCACC TCGGCCTCCC 1200
AAAGTGCTGG TATTACAGGC ATGAGCCACT GCGCCCAGCC TGGACTCCGT CCTTGCTGCG 1260
ATCAGGGGTT CCGTCTCTCT ACCCTGCCCA TGCTGGATGC AGCCCACACA ACCACTGCAG 1320
GGGCAGCTCC CACAGCAGTG GGCACAATGC CTCTGGGAGA ATCAAATACT CAGTGAGATC 1380
TCTGCAATCC AAATCCCTTT CTTATAAAGA AAAGATCATA TTCAGCAAGC AATCTATAAA 1440
ACTTTACCAA AGCAGAACAA AGTTGCCTGC TAATTTCTAT TAACAAAATG ATGTCACCTT 1500
CATGTTAATG GACTGTGTGA AGGTAAGGCT GGAAATTCTC AGAAGGAACT GAGAGTTTTG 1560
AGGCGCCGAA TGGGGGGTGT AGCTTAGCTG CCTCTCACTG ATGCAAACCG ACAGCCCTCT 1620
GTGGTCCTCC GATCAATCTG CCAAGTACAG AACTCAGCCT GGGGTTTTCC CCAAATTTCT 1680
TCTCAGGTTT ACAAAAACTC CCCCCTCCCC TTTGAGGAAG CTGTTCTCAC 1730
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