| Tag | Content |
|---|
EnhancerAtlas ID | HS182-19707 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr7:33769340-33770690 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr7:33769509-33769519 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr7:33769509-33769519 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr7:33769509-33769519 | ATTTTCCATT | + | 6.02 | | POU4F2 | MA0683.1 | chr7:33769350-33769366 | TGCATTAATAATGCAA | - | 6.01 | | STAT3 | MA0144.2 | chr7:33770521-33770532 | TTTCCCAGAAG | - | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAAACAGAAT TGCATTAATA ATGCAAACCT TTTGTTCACT GACTCTTTTC CTTCCCAGCC 60
ACCAGCACTT CAGCTAGAGC TTTCTGGAAG TCCTTGGGGT TTTTCACATG CTCTCGGAAG 120
TGAGGCCAGT AGTGTCTTGC CCAAGTAGTC AGGTCGGCTC CTCCAAGGCA TTTTCCATTT 180
CCTTCCTTCC CCCTGTGCTG GCCTCTTCTG CTGGGTGTGT GCAGTTCCCA TGGGGCTTGC 240
TATGTCTTCC ACTCTCTCTG TCTGCTACTG ACACCTAAGT CCCGACTAGG GGCTGCACTT 300
TGTTCCCCCA AATCCATAAG TGAAATCCTA GCCCTCAGTA CCTCAGAGTG TGACTGTATT 360
TGCAGAGATG GCCTTTAACA TGTAATTAAG TTAAAAGGAG GTTGTTAGGC TGGGCCTTAA 420
TCCCATATAA CTGATGTTCT TATAAGGAGA GGAAATTTGG GCCCAGACAC ACACAAAGGG 480
AAAGATCATA TGAAGACACA GGGAGAAGAC GCTCACCTGC TAGCCAGGGA CAGGGGCCTC 540
AGAAGGAACC AACCCTACCT TGGAAGAAGT TGACACCCTG ATCTCAGACG TCCAGCCTTC 600
AGAATGGTGA GAAAATATAT TTCTGTTGTG GAAGTCACAC AGTCTGGTAC TTTGTCATGG 660
TCATCCCAGG AAATGATTAC AATCCACTAC CAAGAAATGT CTGGCACCTT CATGACGACC 720
AAGCTGGATG TCAAGTCAGG GATGACAGCT TGCAGCTTCT GCTGATGTTT GCCCTCGGAG 780
AGGAGCCCCC AAACCCTGCT GTTTGTGCCG ATGTCATTCA GTGTTTGTGG AGTAGCCCAG 840
GGGTCTCCAA CCCCGGGACC ATGTATCGGT ACCAGTCTGT GGTCTGTGGC CTGTTAGGAA 900
CAGCAGGAAG TGAGTGGCGG GTGAGCGAGC CTTACTGCCT GAGCTCCGTC TCCTCCAGAT 960
CAGCTCACCT GCCCCATTAG ATTCTCATAG GAGTGCGAAT CCTACTGTGA ACTGTGCATG 1020
TGAGGGATCT AGGGTGCATG CTCCTTATGA GAGTCTAATG TCTAATGATC TGAGGTGGAA 1080
CAGTTTCATC CAGAAACCAT TGCCCCCTTC CCCCCTAGTC TGGAAAAATT GTTGCCTTCC 1140
CTCCCTGCAT GTGCCCTGTG CCCTAGTATC TCTGGAGTCA TTTTCCCAGA AGCTATCATG 1200
ACTTTTAGTT AGAGTGAGAG GCTGGGGTCA CTCAGGGCAC CCGGGAATCA CAGTGATCCT 1260
ATGTAGTGGG AGCTGGATCC GTGGAGGAGA TGGACACTGA CTGAAGATTC CACTCCAGGC 1320
TGAGAGAGGA GAGAGGAAGT TCCCTGGCTG 1350
|
| |
|
|
|
