| Tag | Content |
|---|
EnhancerAtlas ID | HS134-14552 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr12:89847000-89849400 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE41 | MA0636.1 | chr12:89848425-89848435 | GTCACGTGAC | + | 6.02 | | BHLHE41 | MA0636.1 | chr12:89848425-89848435 | GTCACGTGAC | - | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I089450 | chr12 | 89843852 | 89849162 |
|
Enhancer Sequence | CTCTTTTACT CCAATTAAGC ATCTTAGGGC TTAACATTTA ACTTCTTGAG TTACCGAATA 60
AAAAATTACT GTATCCACTT GACATTTACT ATCATTTGCA GTTAAGATAA AAAGTCTCTT 120
AACTCTTAAA GGAAGATAAA TTGAGGGAGG CACCAGCTAG GGAGTCCAGA GACCTGGATC 180
CTATAAATGC CTAAGTTCAT TTCCTTTCAT ACCCTTAGAG CAGGGACAGG AGAAACATAC 240
CGCAGAGCCA CTAAACCAGC ACTTAAAGAT ACCATACAAA TGTCTGTTTC CTAATGCTTA 300
GGAAGCAGCC ACAAAGTTAT AGATAAATAC ACCTAGTTTC AGAAGTCATA TGCCCTAAAC 360
TGACAAATCA AATGCCACCA TATAAACTGC TGCAAAGTTT AAAAACTTTA CATTGCGTAT 420
GACCATTTTA CACTTTCAAA GTTGTAAGTT TTAGTTTTAA GACACTGAAG TTCACATACA 480
CTGTGTTCTT TTAGTCTTTC CAAATCTTTG CTTATATAAG CAGTTAGGAA CTGAAATAAC 540
TCTGAACTAG TTACTCAATG TTGTCTAGTA ACCAGGATGA ACTGTTGCCA CAACATTCAT 600
GGAAATATTC TCTCTGTGTC TGCAAGTTTA TTCTTTGTGT GTCCATATAT TTTGTCAGCA 660
CGTTAATATT TTTCAGATAG TATACACCAT ATGACAATCT CCATGAAAGT GTATAACCTT 720
TTTCTTCCTA AAAATAGGCT GATGCAAAAA AACTTTCTGA AAGAGAATCC AATGCACTTT 780
GCTAGAAAAT AAAAATCTAA ATGACATTTA GGAAGGGAGT GTGCTTCCCA AAGTCATGGA 840
AATGGCAGAG TATCTCTTGC ACTGATTCAG CCGATCACTT TTCTGATCCT AGAACAGAAC 900
ACAGGAAAAC CACGATTCTT TTTCTCTCAT CAGCCCCTCT GCCAAAATGA TGCAGAGCCA 960
GGAGATATTC TCAGCTATCC TGAGATTACT CAAGGCTACA TCTTACTGTC CCTGGGGAAG 1020
GGAGATAGGG AATCCCACAG CTGACATTCA CTCTGTCAGG AAATCCTCTT GGCTCTGCCT 1080
TCAAAATACA CCCAGAATCC GATCGCTTAT CACCACCTCC TCTGCTACCT CCCTGGGTCA 1140
AGCCAGTATT GCCTCCCGTC TGAGTATTTC ATTAGCTTCC TAATTAGTCT CTTTGTCCAC 1200
CCCCATCAAC ATCCCCAGCC TGTCCTCTTA CAGCAGGCAG AGTGAACCTG TTAAGACACA 1260
AGTCACGTCA TGTCCCTCCT CTGCAGGAAA CCCCCCAGTG GCTCCTATGT CACCTGCAAT 1320
CTGGCCTTCC ATCTATCACT GCTCCCACTC TCCTGGAGAG CCCTTCCCAG ATAGCCATGA 1380
CTTGCTCCCT TCACTCCTTC AGCTCTTTAC TCAAATGCCA CCCCTGTCAC GTGACTCTTG 1440
TCCTGGCCAT ACTAGCTAAA ATGGCAGCCC TCTACCTATC TTTTCCTCTC TGCCTTCAGT 1500
GCCTTTTTCA CCTTTGCATT CCCTGTACTA TATACAGTTT ATTTTTTAGA TCTGTGAATT 1560
GCCTCTCTCT GACTGGAATG TAGAATGTAG GCTTCTCTGG AGCAGGTATT TTTGTTTCTT 1620
CACATTCTCT AAAGCCAAGA ATAGTAAGTT AATAAATACT TATTCAGAGA CATGTATGTG 1680
TGAGTAGGCA TCCTTCCTGG ATCCCACCAC ATCTGCTGTC AGTTGACTTA GGCAACTTAA 1740
AGATTCTAAA CTAGACTGAT GCATTTTTAT TACCATGGTT CATATGTGTT TGATTTCTTC 1800
TGAAGCAACT ACTTATACCT CGCTTTCCCT CCAGGCACGG TGGCTCATGC CTATAATCTC 1860
AGCACTTTGA GAGGCCGAGG TGGGTGGATC ACTTGAGGTC AGGAGTTCGA GACCAGCTTG 1920
GCCAACATGG TGAAACCCTG TCTGTACTAA AAAATACAAA AATTAGCTGG GCATGATGGC 1980
AGGAGCCTGT AATCCGAGCT ACTCAGGAAG CTGAGGCAGG AGAATCACTT GAACCCAGGA 2040
ACTGGAGGCT GCAGTGAGCC GAGACAGTGC CACTGCACTT CAGCCTGGGT GACAGAGTGA 2100
GAGACCTTGT CTCAAAAAAG AAAAGAAAAA AGAAAAAAAG AACTGGTCAA AGGTTTTCTT 2160
CTAGAGAAGT CCTCTAGCTT ACTGCAGCCC ATTAATGATT TCCTCTGAAT ACTGCCCAAT 2220
AACAATCTTT CACTGACATT TATGTATACT TGACATCTAA TGTTCTGAAA CCAACACTGA 2280
TTTCTTCTTC CTCAGTTACT TCTGTCTGGC TAGGTTGTTT GTTTCTTGAG GTCAGGCAGC 2340
CAGCTTGGTA TCTCCCTCAG CATCTCATGT AATGCCTTCA TGTAGGACAT CTTCAACTAT 2400
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