| Tag | Content |
|---|
EnhancerAtlas ID | HS182-13389 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr2:237847500-237850270 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr2:237848546-237848556 | GTCACGTGAT | - | 6.02 | | TFEB | MA0692.1 | chr2:237848546-237848556 | GTCACGTGAT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATTCTCCCAG GGAGCCCTGA TTCCTTTTAC TGGAAAGTGA TATTAGAAAC CAAGATGTGG 60
GTGCTAGGCA TGCTTGATAC CACTGGGATG TCATTGCTTC TAGGCCCTTG CAGCCAAAAG 120
CGCTTAGAAA TGTATGTGTA CATATATGCA TACCTATACT TATTTCTCCA TTGATCCATC 180
TGTATCTATA TGAGGCTAAA CATGAGTTTG ATGTTTCCAG CTCTAATTCC GTATCACACA 240
AATCATTCCA GCTTCCTCCC CTTGCTTATC TCTAATCTCC CACTGCAACG GGAAGAAACC 300
TGGCTCCTGA CATTCTGCAC CCATTTACTT AAGTGTCCCA TTCTATATCC ATGTATGGTG 360
GTGCAGAGTT GCTAACCCCT AACCCCATAA GAAACATCGC TACCATCTAA AGCAGAGTGC 420
TTGTGAGCAG CTCTCTTTGA CTGTGGTCTT ACAGACTCCA CTCCTTTGCA AAGTCACTAG 480
GGTCAGCACC CTGCACCCTT CAGCAAGGCC GTGCCATACA TTTGCAAGTT AGATTCTTGG 540
GTCACAGTCT GCATTGCATC CTGGCATCCC CTGGCCTCAC TGAAGGCTTG TTGCATTGGG 600
TGCCTTGCTC ATGCACTCTC TGGCTACTGT GATGTGGAGA GACTTCAGTG AGTCAAGACA 660
GAAGACAGGC ACCAACACTG CACCTGGCGA GAGGTTTAGA CCTGGGAGGT GGCCATGGAG 720
AGGAGAATAT GTAGATGAGA TAAATTTTAG ACACAGAGCT ATGGATTTGA ATTACATTTT 780
TGAAGTAAGT ACAAAGATGT CCCAGAGGGA GCATCTCTCT CCATTAAATG TCCTGAAACC 840
AGAAGTCTTC ACCCTCCTCT TCCCAGCCCC CATGACACTG GGTAGGAGGA ATCCTTAATT 900
GTGACATCAC CATACCCCAA AGAACCACGC CTACTAGCAA GCACATCATT ACTTATGTGG 960
ATCTCATCTT TCAGTGCGGG TGGATTGGGT TGTCTAATCA TCACGGGCGC CGGTCATAAA 1020
TACTGCTGTC TGGGCTGTTT TCAACAGTCA CGTGATGTGG GAAACACTGT CACTCACCTA 1080
AGCCATCTGC TCAGAACCAG GAGCAGCTGA GCTAGGCCTG GCAAACGGGA CAATATATAC 1140
ACATTCTGCT CCTTTGATAG ATTTGTTTGG GGAAAATGTT CTAGTGATTA ATGGGCCATT 1200
TCCTTGCTGA TACGCTGCAC GTGTAGCCAT TAACAAATGA TTCCAGTGCA GCCTTGGCAA 1260
AGTCCCTCCT GTGTCATCTC AGGATGCGGC TGGCAGGGCA GGCGGGAGGG GCTGGTGTCT 1320
GGGATGAGGT CAAGGCCCAG GGAAAACAGC CTTCCTTTGT GTTCTGGCTG AGGAGGTGGG 1380
TCTGGTGGGG GCTGCAGGGA GCCCACAGAA GGACCAGGGT GGGGGTCCAG GCTGCCGGAC 1440
CCAGCCCTTC ACTCCCATTA CTCCCAATAA TATTCCTGCT GATGGCCCTG CAGGCACGTG 1500
CTCCTTCTTT AAGGATGGGC GGGCTTTTCT TCAACTCATG ATCATATGTT TTGCTTCTCG 1560
GGGAACTTCT CGTTGGTTTT ACTGGCACTG TCACGGGCCC TGGGTAGCAC CTGGGGACTC 1620
TGTCTTACGA TTAGGGACAA AGAGACAGAG AACTGACAGC CCTAAAGAGG TTTGTCCCTG 1680
GGCTCAGTGT CACCCAGCAA CCAGAAGGGA CCCCTCATGT GGTGGCTTGT CCCTGGACTC 1740
AGTGTCACCC AGCAAGCAGA AGGGACTCCC TCATGTGGTT ATTGGTGAAG GTGAGCATTC 1800
TCAGAGTCCC TGCTGGGACA GTCCCCAAAG AGGCCTCTGC TCATGGGGGG CTCATGGCTC 1860
ACTGGGGCTT ACTCCACTGA GAAGGGAGGT AAGAGAGTCA GGGTGGAGCT CCCACCAGCT 1920
CAGTCTCTTA ACTTGGACTC TGCAGAGCCT CAAGGAGCAC CTCACAAGCC TGCTTCGAAT 1980
GCAGGCTCCC AGGCCTGGGA GAGGTGCACC CCATCCCTAT TGTACCCCCT TCCTGATGAA 2040
AGGAGAGAAA TGATTCCAGG GTTCCAGAGA CTCAAGCAGC TTAGAAATCT CTGCACTGAG 2100
AGCCTACTTT ATCCAGCCCC ACCTTCTGCT CCCATTTCCA TTCCAACTCC CCCTGGCTCT 2160
TCCCTCCTGG CTGCCTGGGA CTCCTCTACC CATTAAGGCT CAGCTCAGAT TTCGCCTTCT 2220
CAGGGATAAC ATCATTAGCC CCTAAGGCAG AAGAGATAGC CTTCTCTGTG CCCCTCTAAT 2280
GTGTCACGTT TATGCTAAAA ATGGCGTTAC CATGCTGCAA TGGGAGTAGC TGTTAGTGAT 2340
TCCCCCAGTC CTTAGAGTAT GGGATTCATG AAGTCAGGAC TTAAGTCTTC ACATTCCTGG 2400
AGCCTCCCAC AAAATACACA CTCAGCAAAG TGCCTGGGAG GAAGCTGTCA ATGAAAATGA 2460
TGGAGGAGCC CTACCCTCTT GTGGGGCTTG CGATAGCGGT GGGGCCTTTT CCTTCTCCTT 2520
TATGGGGTGC GTTAAGGCAC AAGGGAAGTG GAATTTAAGA AGTATCCTTC AATGCTTGTC 2580
AAACTGTGGG TTGTGAAACA ACTTAGAAGG TGGTGGCCAG CATTAGTTTA GTGGAATAAA 2640
ACGTTGGATA GAATACAGTG CAATGGACAG ATAAACAGTG TGCATGTATG TGTGTGTATG 2700
CATGTGTACG TACATATGTG TTTATGTATG TGTTGTGTAT ATACATATAC TTTATACATA 2760
AAGAATAAGA 2770
|
| |
|
|
|
