| Tag | Content |
|---|
EnhancerAtlas ID | HS039-01146 |
Organism | Homo sapiens |
Tissue/cell | ESC_NPC |
Coordinate | chr10:115068500-115070230 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr10:115069417-115069438 | TTCTCACCTCCCCCCACCTCC | - | 6.4 | | ZNF263 | MA0528.1 | chr10:115069420-115069441 | TCACCTCCCCCCACCTCCTCC | - | 6.69 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH10I113309 | chr10 | 115068869 | 115070169 | | GH10I113310 | chr10 | 115070178 | 115070533 |
|
Enhancer Sequence | GTTCATCCAT TGTAGCATAT ATCAGTGCTT CCTTTCTTTT TAAGGCCAAG TAATATTCCA 60
CTGCATGTAA GGACCACAGT TTCTGTACAC ATTCATCTAT CGATGGACAT TTGGGGTTTC 120
CACCTTATCG ATATTGTGGA CATTCCTGTG CATTACTTCG CTTGACTTAC TTTCCACAAG 180
AATTTCTCTA AAGGAATGCT ACTAATGGGG AAAATGGAAT CTCAGAGACT CAAAGTAACT 240
GCCCATTGGA TTGTTTGGGG AATGGGGAGG AAATAGATGG CTCCCTCAAA TGCTGGTAGT 300
AATGCCGAAG TTGGGAGCAG GGGTGAGGAA GGCAGTGAGG GATGGGGAGG TACCCAGAGC 360
TTGCATCAGC AGGAAGCCAC CACTACCCCT GGGCCTGCAG GGATGAAGGG AAGTCGCTGT 420
GCTGCTGGGA TCCGGAGAGT GATATGGGAC AGGGCTGCCT GGCAGGAGCC AAGGCCTTCA 480
GAAAAGAAAC ACACCAGCTA GAATCTACAG CCTAGGGGAA GGGAGCTGGG GGAGCAAATA 540
CCAGGATCTC CCTTTCTTCC AACCCTCCAG CCTCCTGCCA ATGCCTCCTA TTGGCGGAAG 600
CCGAGTGGAA GCCGGAGGGT GGGGGAGCCA GGCTTCTGGG CATAGAGTGA GTGCAGGAGG 660
ATGGAGAGTG AATCTGGAGG GCAAACTGAG CCTGTCTGGG ATAGCCTTTG TCACACATGT 720
CACACAGCCA GAATCAGGAC TGAAAGGGGG ATCTCTGACT CCAGATCCCA TGCTCTTCCC 780
AGTCCCAGAG GCACCTGCCA AATGACACAG CTCAGACTTT CTACTGCTGG GGCCTTTATT 840
TCCCTATCCT TCTGAAGGAG AGATCCCAGG GAGGCTGGCA TTTGCAAAGG TGCAGGACCT 900
GGTTATTTGG CCTTCTCTTC TCACCTCCCC CCACCTCCTC CCACAGGGGC CGCTCAGGGA 960
GTTGGACCTC CAGCACTTTC CCCGCTTTGC TGTGTAACCC GCATCTGCAC ACCAAGTGCG 1020
GCAGACCAGT GGGCCCCTGG GGGCTGGGGG CTTTTCTTCT TTCTCCCTTG TTCCTGTTCA 1080
TTTTGGAGCC GTAAGAGAGC CATGGAGAGA AAGAACTGAG AAAATCAAGG GCTGAGAGAC 1140
TGTTGTGAAA AGAGTCCGTG GAGACAATAC AGTGAGTGCT TAGTGAGGTC CTGAATGCAG 1200
GGCTTATGGG GCTGTGCTGA GCCCTCAAAT AGGCCTTTTG TGCTCCTTTC TATTGACTGT 1260
TACTAAACCC TTCAATGGGC TCCCATTGTG CTTGGAATAA AATCCAAACT CCCCACCCAG 1320
GCCCACAGCG CTCCAGCCTC ATCTTATACG CTGGCCTTTC TCTTCTCCCC ACTTGCCTTC 1380
CTGCAGCTCC TGGGCACACC CAGAAGTCTC CCACTTCTGG AACTTTGTAC CTGCTGGCTC 1440
ATCCTCTGCC CGGGCTGCAG CTTCTTGCAT TCTCCCCAGG GATGGCACCT TTTTCTGCTT 1500
CAGGTCTTGC ATGAAACATC ACCCCCTTAG AAAGGCCAAG TTTTCTCTTT TGGTACCTCT 1560
GTATTGTGCC TGTCTCGCCC TCTAAGCTGT CAGCTCCATG ATGACACGGA GCTCGTTGGC 1620
CTTGTTTACT GCTTTATCCT CAGTCTCTAG CAGAACCCAG CATAAAGCAA GCACTTGAAA 1680
TGTGCTTGCT GAATCAGTAA ATGCAGGTTA TGCTTCACGG CAGAAGTAGA 1730
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