| Tag | Content |
|---|
EnhancerAtlas ID | HS052-31867 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr6:1337340-1338760 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr6:1337674-1337689 | GAGGTCAGGAGTTCA | + | 6.22 | | SPIC | MA0687.1 | chr6:1337555-1337569 | TTCTTCCTGTTTTG | - | 6.03 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGATCTCAG CTCAAATGTT ACCACTTCCT TTGAGGTTTT CTCTAGCCAC CCTATCTAAA 60
ATTGGGAAAA AAAAAAAAAA GTCCTCTCCT CTTTTATCTC TCTCTTCTGC TTTATCTTTC 120
TCCTCGGCAC TTGGCATTAC TGAGTTTACC ATATGTACCT ATCTTTGTTT CATGTGTCTT 180
TCACACTTGA ATGAAAGCTC CAGGAAAATA GGGATTTCTT CCTGTTTTGT TCACCGCTGT 240
ATGCCCAGAT CTTAGATTGG TGCCTGGTGG CTGGGCACCA TGGCTCACAC CTGTAATCCC 300
AACACTTTGG GAGGCCGAGG CAGGTGGATC ACCTGAGGTC AGGAGTTCAA GACCAGCCTG 360
GCCAACATGG TGAAACCTCA TCTCTACTAA AAATAAAAAA TTAGCCAGGC ATGGTGTCAC 420
TTGCCTGTAA TCCCAGCTAC TTGAGAGGCT GAGGCAGGAG AGTCTCTTGA ACCTGGGAGA 480
CGGAGATTGC AGTGAGCCGG GATCGCACCA CTGCGCTCCA GCCTGGGCGA CAGAGCAAGG 540
CTCCGTCTCA AAAAACAAAA ACAACAACAA AAAAAAGATG CCTGGCATGT CAAAGTGCAC 600
TCAATAAATA GTCACCAAAT GAACCAATGG ATGGCAATAA TGTGCTTGCT GAATGTGAAG 660
ATAGCATAAA CCCAGGCGGG TGGGGGAAAT ATTAGATGGC AAAGTCAACA ACCAAAATTA 720
TCTTGACAGG TGAGAACGAC AGTCCGAAGC CAGCAAGATG GAATTTAACA GGCTATGTAA 780
ATCAATCCCA CAGTTAGATT TCAGAAAAAC AATTGCACAA GAACAAGATG GGAAAGATAA 840
TGTGGCTAAA TAATACCACA TGCAGAAATG ACAGGGTCTC GGATGACTGC CAGCTCAGTC 900
TGAGTCAAAA ATAAAACCCT CCTTTCAAAA AAGTGTGATC TTTGCTGTCA TCACTAATTA 960
AAATAATCAT AGTTTTCAGC ACAAAAGTGT GCTCATATGC ATTCCTGCAC TTGAACTCAC 1020
ATCTTTTCAT AGATACATGC AATATGCCTG TGATCAAGTT TATTCATTCC AGCCTGGTTT 1080
GTAAGAGCAA AGATGAGAGT CCACCTAACT GTCCATCAGT AAACAGGGGA CTGGTGAAAT 1140
AAATGAGGGA AAGCGAATAC AGCCTTCAAA TAAGAAGGAG GAGCCAGGTG TGGTGGCTCA 1200
GGCCTGTAAT CTCAACACTG TGGGAGGCCG AGGTGGGAGG ATCTCTTGAG CCCAGGAGTT 1260
CAAGACCAGC CTGGGCAACA TGGTGAACCC CATCTCTACA AAAAATATGA AATAGAAAAT 1320
ATTTGTATGG TGACGCACAC CTGTAGTCCC AGCTACTCAA GAAGCTGAAG TGGTAGGATC 1380
ACTTGAGCCC AGGGAGGTCG AGGCTGCAGT GAACCATGAT 1420
|
