Tag | Content |
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EnhancerAtlas ID | HS182-06897 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr14:102630070-102631060 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr14:102630134-102630152 | GTTTTGCTTTCCCTATCC | - | 6.31 | Nr2f6(var.2) | MA0728.1 | chr14:102631018-102631033 | TGACATTTTAACCTC | - | 6.26 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGGATAACC CAGAAGGAAG CTTTACATAG TGTCTTCATT GCCTGAAACT AGCTTTGTTT 60 GGAAGTTTTG CTTTCCCTAT CCTGGTGTCC TGGAGAAAAT GCTTGCACTC TCCCTTCCAG 120 AAGCAGGTGG CTTTGCTGCT GTCTCTACTT CTTTCCCATT AGTTGCAAGA ATTACACTAC 180 TCCTTACATT GCCTTTTTCC TCCCTTTAAA TTATAGAATC GGTGTACACG TAGTTAGCAA 240 GACTGAAGGC ATTATTAGCT CAGCTAATTT AAAAATGATG GCTGTTGTGC TCAGGGCTTT 300 CCTTGATGTG GCAGCAGTCT GACTTTGCCA GGGAGCTCAG AGAGTATCTC ACAAGTTGAG 360 CTGGAAAGGG CTTCACAGAA CCCTGACTGA TACACTGGAA GTGCCACATT AGACCAGGCT 420 TTGGTCCATT TGCCACTCCT GGCATCCCTT TGGAGCCTCT ACCCTTAGAC TCATGACACC 480 TTTCTCTCTC TTCCTCATGG CCATATATTG ACTTCCCAGC CACTTTTAAT CATTGAAGAC 540 TCCAGTGCCT GACTCACAGC CTTCCTTTCC ACTCCAGTTC CCGCCATCAT CTTGGGTGGT 600 TTCATCTTCA TCACATGACC CAGGAAGTAC CTTGGTGCTA GCTTTCTTGG CTTCCATGTC 660 CACCCTACTA ATCTCCTCTA GTCCACCTCT GGCACTCTCT CCCACAGTGA CATGCGGGAT 720 CTTGTCATCA GCTGAAATGG TTTAGCTCCA AAATCGCTAA TTCAGATAGA AACAGCCTTC 780 TACTGCAATA TGGCCTTGCT TCTCACTGCT CTAATTTCTC CAGGATACTG ATGACTCAAC 840 TTCATGTTGC CAGATCCATT GGACACCGCT TGGCCCACAA CTTCCTTGAC CTCTCAGCAG 900 CATTTGACAC AATTGATCAT CTTCTCTTTA TTGAAACATT CTTTGTCTTG ACATTTTAAC 960 CTCAACTTTT TTTTATACAT TTTTGACCCA 990
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