| Tag | Content |
|---|
EnhancerAtlas ID | HS182-05398 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr12:112007430-112009090 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr12:112008864-112008875 | TTAATCCTCTT | - | 6.14 | | Crx | MA0467.1 | chr12:112009056-112009067 | AAGGGGATTAG | + | 6.32 |
|
| | 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 |
| GH12I111569 | chr12 | 112007197 | 112009194 |
|
Enhancer Sequence | GATCACTTAA GCCCAGGAAG TCGAGGCTGC AGTGAGCCAG GATCATGCCA CTGGACTCCA 60
GCCTGAGTGA CAGAGCGAGA CCCTGTCTTA AAACACCACC ACCACCACCA CACTCTTCAT 120
ATGAAGTTTT ACCCCTTCAG TGCCTTTACC CCTTGAGTCC CTCTAGAGAA AGGGATAAAA 180
GGCTTGGTCA TGAAGCCATG AACAACTAGA TCCAACCTAG ACACACCAAA AAATCCAAAC 240
AACTCAGGTA GAAAAGGATC TTAGGGCTCT AGTCCCATGC TGTCCAAGAG AACTTTGTAC 300
AATGATGAAG ATGTCCTATG TCATGCTGTC CAATATTGCA GCCATTAGGC ACATGTGGCA 360
GCTAAGCACT TGAAATACGA TTAGTATGGC TGAGGAACTG AAATATTTAA ATTTTAATCA 420
ACATAATTTT AAATTTAAAG AACCATGTGT GGAAGTAGCC ACAATACTGG ACAGTGCCCA 480
TTCCCATCTT CTCGAGTTCT CCAGACAGTA AGCCACCCCC TTCCACGGCA TTCATATCAC 540
CTCTGACTTA TGCACCAAGA ATGCTTCCTG ACAGGAAACT CAAGTCTCTC CCAACGATCT 600
ACCCGTTGCT CATAAACTTA TCCCTTTCTG GAGGCCACAA AACAATTGTA TTCCCCTTCA 660
AAAGACTATC AGTGGAGGAG AGGGGAGTAT AGCTGAAACA ACGTTGGCCA TTTACTGATA 720
ACTGCTAAAG CTGAGTGACA GGTACATAAG ATTCATCCAG CTGTTCTCTT TCTAAATACG 780
TTGAAATTTT ACATTTTAAA AACCTTATTA GCGTTTACTT TAAGCTCATT TCATTTTCTA 840
ACTGAAACAT ATTCTTCCAA ATGTGTTTCC TTACTTTCAG TGAGGACCCC CTCCAATTCT 900
TCTATCACAC TGTGAACCAA ATTTTTTCTA CATACACCAT GTGTATAGCA ATCCCTGTAC 960
TTTAGCACAA ACTCTTCCCG CCTGGAACTT CCTCCTCTCT TCATGGCCTT ACTGAAAACT 1020
GCTTATCTTC CTTGAAGATC CATCTCAACT CTCATTATTT TGAAGCCCTT TTTCTTCACT 1080
GCCCACCCAT GGCAGTCCCC TCCCAGTGCT ACCAATTTAA ACTATCTGCA TGCCTGCCTT 1140
CTCTACTACA CTGGGTAACC TGGAAGCAGA GATAATGTTT CATTCATCTT TGTCTCTGTC 1200
CTAGTCTGAC AGCATCAAAT GTGTAATGAA TTAATGAATA TACAAACTTA ATGAAACGCT 1260
AAACTGTAGC CATTCATACT GTACTACCCC AAGCCCATCA ATACCACTTT TCAACCTTAA 1320
CTTGCTGGTG TAGTTTCTAC TGGTTTCCAA ACATGCTAAT AAGAACAGCT AAAAGTTACT 1380
GAGCACTTAT TACTTGCCAG GCATTGCTTT AAGCGTGTTA CATGTTTAAT TCATTTAATC 1440
CTCTTCCATC CCCTTTTTAC AGGGGAAGAA ACTTAAGCAT AAGTGAAAAT AACTTGCCTT 1500
ACATCACGAA GTATGAAGGA GCAGGGATGC GAATACTAAT TGTAAAGTCC CTGCTCCTGT 1560
GTACAACAAG GAAGACAAAT CATAATCTCA AATGCAAGCT TCAAATCCCA AAATTCAGAT 1620
TTGGGAAAGG GGATTAGGAT GCCAAATAGG AATACTGACC 1660
|
