| Tag | Content |
|---|
EnhancerAtlas ID | HS182-06013 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr13:101195730-101197310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr13:101196405-101196426 | GCCACTTCCCCTCCCTCCCCC | - | 6.42 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH13I100543 | chr13 | 101195951 | 101196938 | | GH13I100544 | chr13 | 101197241 | 101197390 |
|
Enhancer Sequence | TTGCAGGCAT GAGCCAGCAC GCCTGGCCAA CACCAGCTTC TAACATAAAA ACCACCTTTA 60
TAAATGGTGC CTCAAGAAAA TATTCATCTT TATATGAAAA TTTCATGACA GGAGGAAATG 120
TTAGTAAAAT CTGTATGTCA TCATGTCAAA GCATCTGTTT TCTCCACATG ATATATCAAG 180
CCAGTAACAA TGCATACTGC CAGTTGGCAA GTTAAGACTT TGTTAGAAAA AAGTAAAATG 240
ATTTAGACTT GGGTAGCATG AAGCTCAGGC CCCTGCCAGA GGGGCTCTGC CACTGGCCAG 300
GGAGAAATAG TATCAGAATC ATAAACTCCT GGTCCAGAAG GTGGCATGGC AAAGAGCTTA 360
TCTCTATCTT TACATTTGCT GCATTAATTT GCTTTTGTCA TTCAATACCT CGTGTCAAAA 420
TTGGCCCCAG CAGATCCTGG GCCCACCAGA CTCACGAAGG GCATGGTGAT CACGGCTGTA 480
CACTGGTTTC AAGGACACCA ACTGCTGCTC TAGTCCTTCT GTGACCACCA GCAGCCCCAC 540
ACTGTGCCAG CCCTGAGCAA ACGCAGCCAT TCTACATGGT GGAGATGGAG TAAGAGTCAC 600
ATGCGATGTT GTGCACGTTT CCCCTAGAGA GGGTTTTTCT TACTTTATGG AAACCTTCTT 660
GTGTCTCATC AAGTAGCCAC TTCCCCTCCC TCCCCCACTG TAACATTATT TTCCCTGGAG 720
AAAACGCCGA GTGTCTGATA TAGTTACACA TTAATTCTTC AGAAGTTTCT TAGAACTGTA 780
GGAAACAGGT GAAAAAACAA AATGCCTTGA ACTTTCAACC TGTGCCTGGC CTGTGTGCGC 840
GAGGCGGGCC CTAAGGTCAC TCTTCCCCGC GCGGCTCGGG GCAACGTGCC AGGGAGGGCT 900
CGGGCCGCAT CCTGTTGGCT CTTTGATGCT TTCGTTTTGT CGCTTGCTAG TTTCTTTACA 960
GCAAAGGCAA GGGCTTCCTG CTAAGGCAGA CCCCTCACCA GCCCCACTGC ATACCCCGGA 1020
AAAGTCCCTG GCAAAACACC TTTCTTCCAT TATCTGCACC GGCCCCGGTA AAACGCTGGC 1080
GCCTTTGAAA TCAGAGGCCA GGGTCTCCTC TTCACAGTTC GCTCAAGACA CTGAACACTT 1140
ACGGGTCTGT GAAATCAAAC GGACACTTGG TCCCTGATGC CACCCCAGGC CTCCTGAATG 1200
CTCCTCAGCA ACCATCCCTT GAGTTTTTAC TCTTTGGCCA TGCCAAATAT AAATAACGAT 1260
TTTTTTCATG CCATATCACT TTAAAGGCAA TTGTGTTGCC ACCTTTAAAA TGTTCAGTGA 1320
CCAACAACGC AGACATGACC ATCCCCTGCA TCCCCATGTC TGCTTCAAGT ATGGAAAGGA 1380
ATCACTGGAA AATCCCAAGA TGCCAGGCCA GGGAACGAGC TCTATGCAAA CAGGCAGGAT 1440
GGAGAACCGG CCAGGGCCAT GGCCCCAAAT TCCAGGCACG GCAGCAGGAG CGGAGGTGCT 1500
GCCAGCCCCT GCTGCCTCCT GGTGTGACAC TCAGAAGGCG CAGCGGAGGC GGCAGCAGGA 1560
GGCAGAGCCA GGAACACATG 1580
|
