| Tag | Content |
|---|
EnhancerAtlas ID | HS182-00392 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr1:21872460-21873690 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Tcf12 | MA0521.1 | chr1:21873418-21873429 | AACAGCTGCTG | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACCATGCCCA GCTAATTTTT GTATTTTTAG TAGACACGGG GTTTCATCAT GTTGGCCAGG 60
ATGGTCTCGA TTTCCTGACC TCGTGATCCA CCCACCTCAG CCTCCCAAAG TGCTGGGATT 120
GCAGGCAATT CTTTTAAATT TAATTCAGCT GAAGTTTTTC TTTTATCAAT AGGGCTAATA 180
ATCCCCACCC TGCCAGTATC ACTAGGATGT TGTGAGGATC TGACGCAATT TGAGTTACGG 240
GAATGTTGAG AAAGAAAAGG GCGTAATGGA GTAACGAGAT TAGTTTTCCT GTTATGGTGA 300
GGTCAGTGGC CTTTCTGGGG TCAAGAAGAG GGGACTTTCC TTGGCACCAA GAGGGTAAAA 360
GTGTCTCCTC CTGACCTTGG GTATTTTGGA CCATGGGATC TGAGGTGTAC CAGGAGACAG 420
GAAGTGTGAT CAGAAAAGGC CTGGTCTAAT GGTGCACAGC TGTGCATATC CAAGTGGCTT 480
GACCTCTCTG GGCCGTTTCT GAATCTGTGA GATGGGAATC ATAACCACTC TCCTGACTTC 540
ACAGGATGTT TTAGGAGAGA TTGGATCTGG GTTGGGGAGA CAATTTTGGA AGCAGAAAAG 600
GCCCCTCCGT GCTGGCAACA GCTCGTCCAC CTCCAGCCTG TGTGTGCTGC CTCCTGGGTG 660
ACTGCTGGCT TTAGGCCAGC GCCTGGCAGG GCTTCACTAA AGCCTCCGTA GGCTGCTGCT 720
ATCTCAGTTC TGAGGTACGG GCCGTGGAGA CCCCCAGATT TGGGCTTAAA TCCCAACTCC 780
ACCATTGCAC CTCTGAGCCT CTGTTTCTCT GCAAATGGGG ATACTAGTCC CTAGCCCAGA 840
TGGGGCCTGG TACACAGTTG GTGCTCAATA AGAGCAGTTC GTCTTCTTCT GAGCATGGGT 900
GCATCCCTCT GGCTGGGGTA AGCACCAACT CAGATTTCTA GGCCCATAGA TGGGCTGGAA 960
CAGCTGCTGC TGTTAGGGGA AAACCTACTG TGTTACTAGC CAAGGGGTTC CCTTCCATGT 1020
TTTTGCCCCA CAGGGCACCT GGCACAATGT CTAGCATACA GTAGGTGCTT TGTCCACACT 1080
GGCTGGTCAG TTACCTCCAA GCTGACAGAA ACTCTGTCCC GTTCCCGACT GTTTCCATAG 1140
AACCTAGCAC AGAGATACTC AGCAGGTGCT CTGTAGGTGT TTGGGAGTGA GGAATGAATG 1200
AACAAAGTTG AATGAACAAG CATCGGGCCC 1230
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