| Tag | Content |
|---|
EnhancerAtlas ID | HS136-14282 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr3:184190380-184191420 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr3:184190584-184190598 | CCCGCCTCGGCCTC | + | 6.01 |
| | | 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 |
| GH03I184472 | chr3 | 184190102 | 184191812 |
| Enhancer Sequence | GCCCAGGCTG GAGTGCAGTG GCATGATCTG GGCTCACCAC AACCTCCACC TCCCGGGTTC 60
AAGCAATACT CCTGCCTCAG CCTCCTAAGT AGCTGGGATT TCGGGCATGC GCCACCATAC 120
CTAGCTAATT TTGTATTTTT AGTAGAGATG GAGTTTCTCC ATATTGGTCA GGCTGGTCTC 180
AAACTCCTGA CCTCAGGTGA TCCACCCGCC TCGGCCTCCC AAGGTGCTAG GATTACAGGC 240
GTGAGCCTCC GTGCCCGGCT GAAGAATATT TTCTAATATA CAATTCATAT TTAAGTTCCT 300
CATTTGTGCC CACTGTTACT TTAATAGCAT TTGTTTCAGA TCCTGGAACC AATCAAGAGT 360
ACATATTATA GTTCGCGATT ATGTTTCCTT ACTCTTTTTT AACCTAGAAC AGTCCCCTTC 420
CCCTGCCCCT TACCAATATT TTGGTGGTTT TTTATGTCAT TACATTTCTG AAGAGCTCAG 480
GCTAGCTCTC TTGTGGAAAT TTCTACACTC TGGATTTATC TAATTGTATA AAGCAGGTTC 540
GGCATTTTTC TAAAGAACAC TTCCTAGTTA ATTTTAAGAT GGCGTGACAT CAGGAAGCAG 600
GTGCTTCCTC GTGATTAGAT CCCGCCTGTG CACTGTCAGC AGCAACATCA CATGCATAAA 660
GCTGCATCCT TTTCAGGGCA GCACACTCAG GGACCCACAT GTCCGCCTGC TTTTCATGGC 720
TGATGTTGAT TTTGACTACC CAGTCAAGGT GCTGCCTGCT TTATCCACTT ATTTTTCCCT 780
TGCAACTAAT AAGCCATTTG GGGGGAGAAA TGTTAAGACT ATGTAGATAT TCTGCTCTTC 840
GTCAAACTTT GTACTGTTGA TTTATCACCC ATTTTCCTGA CCTAGGCCAT ATCCTGCTGG 900
TTGTAAAATG ATGGTTTTCA AATTTAACCA CTCCCTCTAC ATTGATCAGC ACTTTCTGGC 960
TCTACAAGAT GTTCTAGACT CATCTTGTAC TTTCCATATC CTAGTCCTAG AATCAGCCAC 1020
TTCTCCAAGA ATCCCTGGTT 1040
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