| Tag | Content |
|---|
EnhancerAtlas ID | HS182-14348 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr21:27526240-27527360 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr21:27526582-27526593 | ATGTTTACATA | - | 6.32 | | Myog | MA0500.1 | chr21:27527165-27527176 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr21:27527165-27527176 | GACAGCTGCAG | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACTTTCAATT CTAAAAGTTC ATCCATCATG CATGCTTCAC GTTGTAAAGC AAATATTTCA 60
CAAAAATGAG TTTACAACAA AAGAACACCA ATCCCACTTC TCCAACCCTC CATGTCAGGC 120
AGTAAGCTTT CCACATTTGC TTACATTCTG AAAATAACTA TTTTACATGC CAGGAATGCA 180
ATAGGCTTAA GCTGTCAAAA AGTATCATAC TTTAAGTGTA ACTGGGTAAG AACTATGGGC 240
ACACACACAA TAAGCCTTCC AAAACAAGGG GAGGTAAATG AAATCTTAAT ACCTGTGTTT 300
CCAGAAGCCC AGAAATGAAG TGCAATTCCT TATAATCTGT ACATGTTTAC ATACCCATAC 360
AGACAATAAA ATGTGTAAGG TAATGACAGG TCCATCTCTC CCCTTCCTTT TAGTGGGCAT 420
CTGACATTTC AGGGTTCAGA ATCACATATC CTGGGTCCCA AAAGGTCCCC CCATTCCTAT 480
TCCAACAGTG CTCACAATAG AAAAAGATGA ACTGATCACT GGACCCTACA TCATCTCATA 540
TATGTATAAT ACTAGTCCAC AGAGAGGTTG AAGATATGCC TGGTAACTCT ATTCATCCTA 600
CCCCACAAGT TTTGTCCAAA TCAGGCCATG CCTTCAAGTG GGCCAGATTG TCTTAAAGCT 660
CCTGGCTTAA TATTTAACTG ATAGCAACAA CCTAACGTTA GTACCTTAGT AACTAAAGGG 720
GATGCAGCAA CATGAAGCAG AAAAAGTGAT GAAGAAAGAG ATTAGAAGTT AGAGAACAGG 780
GACTGGGCTC TTGATCCTTA AAATGTGGGT GATTTTGAAC AACTCAACAT CTCCAGATAT 840
TACTTTCTTC ATCTGTAAAG TGGAGAAGCT TAAAAAGGAG GTCTTATAGA TTCTACCTGT 900
TCCAGAAACT ATGATTCTCT TCCTAGACAG CTGCAGGTTG AAGAGACTCT CCTAGAGCTG 960
CACTGTCCAA TACAGTAACC ACTAGCCATC TGTGGCTACT AAGTACTTGA CATGCAGCTG 1020
GTCTGAATTA AAATATGTGA AATATGTAAT CAGGTGCGGT GGCTCACAAC TGTAATCCCG 1080
GCACTTTGGG AGGCCAAAGC GGCAAGTCAC TTGAGGTCAG 1120
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