| Tag | Content |
|---|
EnhancerAtlas ID | HS182-09056 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr17:10098510-10100030 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat4 | MA0518.1 | chr17:10099892-10099906 | CCCTTTCCCGGAAG | - | 6.95 |
| | | 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 |
| GH17I010196 | chr17 | 10099377 | 10099732 |
| Enhancer Sequence | TTGCCCCAAA AACCAAGACC TCCTCCAAGC TGGCCTCCTC CCAAGGGCTA GCTGGCCACT 60
GGGTCAGATC TGGTGACTCT CTTGGAGTTA GCTCCCAACT CCCCTCCCCC GTGTATGCTT 120
CCTGCAAAGG CTGGGTCTCT CGGTTCCCCT TGCTTCATCT GAACAAGGAA GATCTCCTTG 180
GGAAGTATCC AGTGTGCACA CAGTATTCAG TGCCTCCCTC CCCTCCACCA AGATGGGGTT 240
TCCTAGTATC ACTCTTTCTA TCAGGGTGAA AGTTCCGCTG GAGTAGGGAG CACATTAGAG 300
ATGCCATATT CATCTGTGTA CCCACAATCC CATCCCTAGG CCAGGAGGCT AGTACAGTCC 360
ATCTGTCTGT ACTTGTTTCT CCAACAGCTG CCCTGGCCTT CTGAACTCCA TGCTCCCAAG 420
CAAGCTGAGT GACAGCACCA CATTGGCTGA CATCTCATGA GGTTCGCCAT CTCCAGTATC 480
TATGGGCCCC CTCTCTAGTC TCATGAGTCC AGATGCTGGC CAGTCTACCC ACCAGCCTGG 540
GGACCTCTGC ATTCTCTGAG TCTGCCCTTC AGGACTCACC CCATCCCAAG CAACTCTGCT 600
TGCATGTCCT CTATCTCTAC CTAGCCTTCA GCCTTGAGGT CCAACTTGCT CATGTAGGAG 660
GTTCCCAGAT GCCAAGCACC TGACCCACAT GCCCCCCTGT TGAAACTGCA TCTGCTTTGG 720
CCCTGAGAAG AGTCCCACCC AGTACTTAGG ATACAGGACT CGGGCCCACT GTGGGAAGAC 780
CCCCAGCTGG TTCTGAGTAA AGTCACACTT TGGGGTTAGC AGGGAAGATC CTCCAAGTTG 840
CTCCTGGATG CAGCTGTCCT CGTTTTAGCC CTAGAGGTTC AGCCTCCCCT TCGCGGTGCT 900
GTCACCAACA TGCTGACCTC AGGGGCTGCG CATGCCCCTT TTCCCCATGG ATCCAGACCC 960
TTCGCTCACA CGCTGTTTGG CATAGTTGAG CCCGGGCTAT CATGTTTAAA AAAGGCACAG 1020
GCGCAGGGGG TGATACTCAG TCATCTGAGC TGCTAACAAA ACACGCAAGC ATTACTAGTT 1080
GGGGAGCTGA CTTCGCCTCT CTCATATTCA GCTTGCTTGT CTATAAAATG GGGGAAGTAC 1140
CTCACCCTTC ACAGAGCTGT CAGGGAACTG GTGATAACGT GCACACACTG TGCCAAGCAG 1200
GTGCTCAGAA GTATTGCTCA CGCAGATGGA TGCTTCTGTT GCAAGTTACT AGTCAGGAAT 1260
GGTCTGAGAG GCCCTGAGAC ACCAGAGATC TCTTACCTTT GTATATGCCA GAGGATGGGA 1320
CAGACACACC CAAAACTGTC CCAGTTGTTA ATTCCGCTTG TCCCCTGGCC CTGGTCCATC 1380
GTCCCTTTCC CGGAAGAAAA AGCAGCACTC CACTCTTGCT AACTAACACC TACCCAGCCT 1440
CACCCCTACA CAAAACACAG CTGGCTCAGT CCAGCCAGGG ATGCTCCTCA CCGGACAGAC 1500
ATCCATCAGC CAAATTTCCA 1520
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