| Tag | Content |
|---|
EnhancerAtlas ID | HS060-10802 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr14:100747510-100750120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr14:100750061-100750075 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH14I100281 | chr14 | 100747604 | 100748462 | | GH14I100282 | chr14 | 100749161 | 100749310 | | GH14I100283 | chr14 | 100749381 | 100749530 |
|
Enhancer Sequence | ACCTGGAAAT CAGCCTGGCT TGGGAAATTC ATGTTGTTGA TCTTTAATTA TTTAATTATT 60
CTTTAATAAT CCTTCTATTT TCTTGACATC TGACCCCCAG CAAGAGTAAG GATCCCAGAG 120
GTCAAAACAG TGGTGAGAGC CAAGCTGCTC ACAGACACCC ACTTGATGCC ACAGCCATGC 180
CATGAGGCTT CCTCCCAGCT GCTCTGCTGG CTTGCTGAAG CCAGCTCTGA GTCACAGGGT 240
TGCCTTGGAC CCTCGGCTGT AGGGGGCACC TGTCTGGCTC CGGGCCCTTT GTCCTGGATA 300
CACTGACAGT AATGTGAGCG CAGCACTTCA GAGTTCAGGC CCAGCAGGTC CTGGCAAGTG 360
CATTCCACCC GAACTTTTAA CCCAAGCGGT GGGGAAGGAA GCCAAAACTC CAAGCTGCAC 420
TTTCTTGGGG TTCTGGCCAT GCACTTCTTA GCCTTCTCTC TGACTTTACA GGACAAAAGG 480
TACCCCACGC CTTCAGAATC ATGCTTACCT GCACGGCAGC ATCTGACTGG ATGGCTGGCT 540
AGGTCTCATC CACCCCAAAT TACTGACCCT TGATTTATGT TGTTACTGCT CAGGTTATGC 600
TCAGATGCCC TGGTTGCCTG AAGATGGTTT AAGTGCAGGC CCTTCAGACA AGTCACGTCA 660
GGCAAGAGAG GGCTGGCCTC TGACCCACAA GAGGGCAGAT TTGTGGCCAA GAGGCTTCCT 720
GGCATCCACC CCCAGGCCCA AGGGATCAGT GTGGTGCCAG AGAGGATCTT TAAGCTGGGA 780
CTGTACTGAG GCTTGATGGG AAGTATGGGC AGCATGTACT TGACACGTTA TCACCCAGTC 840
CCCTTGTAAA ATCTGGAATG GAGCGTTTAA GCTGAGCGTT AGCATCAGGT CAGCAGGCAA 900
AGCAAACCTC CCACAAACTG GGTGCCGTAA GGTGGGAGGT GACACATGGA GAGCTTCGTC 960
CTGGCCGAGC AGGCACCCAG CCCCATGTCC CCCGCCAGCA TTCTGGATGT CAGAGGAGGG 1020
TGCGTGTGAT GGCGTCACAT TCATCTGAAG CACACTGATT GATTTTCCAC AAGGTGGCAA 1080
GTTTGATCAA ATTGACCGCT TTTCATGAGA CACCCAGATG CTGTAAAAAA AAAAAACAGC 1140
ACTGGGATGT GTTGAGGAGG GGGCAGTTTG CTGTGCTCTG TTCTGTCTGC TGCTCTCTCT 1200
GGGGGCCGCA CAATGTCCGC ACACATCACG GAGGGGAGAA AGGCATCAGT ACCAAACGGA 1260
ACAACCTCTT TTTTCTACAT TGTCCATACC CGGACATGTG AGGCTCTATT ATCAACAGGT 1320
GGTGAGAAAA ATTATGTTTT TATTCGCTTT CTGGTAACTT CTGTAGGCCC TGGCTCAAGG 1380
ACTTAGCATT TCGTCTCATG TACATCTTTT TCTTAAGTGT TCTTTGCCAT TTCTGGAATT 1440
GTCCTTGGTT TTTCCTTAGC TCATAGGTCA TAGATGCAGA AATATAGTAT TTAAGGCATC 1500
CGCATCCAGC ATCAGATGGC TTTGCATCCA GAAAAACATT GATAACTCAG TTTGAAGCAC 1560
CAAGCATGTG TAATATGGCT CTATACAATA TAATAAATGC ATAATGTTAA GCTTTTTAAT 1620
GCCTGTGGTT CTTGTTTGTT CCTCAGTCCT CTAAGCCACT TCTTTAGTGT TTCACTGCAC 1680
ATGAAACCAG GCCATGAGCC CTTCCTGGTC TAAGAGTTGC CTAAACTGCC CGGGGCAGTT 1740
CTTGCGGCTT GCTTTCTCAC ACACAGGACT GGGAACTCCC AGGATTTGGT CTCACACCAG 1800
CAAGAAATGC TTCTGTAACC TTTCAGCTCC AAGGTGGGCT CAGGAGCAAG AGGGCGTTTT 1860
AAAGAGAGCC TCACCCACTG TTCAGAAAGC ACAGCCCAGT GAAATGCCCA CGCAGCCGGA 1920
CCTATGAGCC CATGTCAGCC CTGGAAGCTC CGGAGCTAAC TGGGATGGAC TCGGAAGAAC 1980
TTGACCAAAT ACACTGAGAG CTACTTAGGA TTTAGCCAAA AGCAAAATGC AGAGCAGAGC 2040
TTCCTCCCTC TGGTTGGGGC CTTGGTGTCT GATGTTCTGC AGAGCAAGGT TCAGAGTGAG 2100
GCGTGAAGTT CATTATTACT TGAATACATG TGACTTTCCC TTTTTGCTAG TGACAGAAGG 2160
GGCTGCTGAC AGAATGCTAC TGAGGTGGCA AGTCGCAGGC CTGTGCAAGC CCAGAACTGC 2220
TGAGTGAAGG CCCTAAGTAG GGCTGAGCTG AGCAAGACGG TGGAAAACCT GTAGATTTTA 2280
CATGGGAAGG AACTAAAGCT TTGGAATTGC TTTTTTTTTT TTTTTTTTTA GATGGAGTAT 2340
TGCTGTGTCT CCCAGGCTGG AGTGCAGTGG CGCGCAATCT CAGCTCACTG CAACCTCTGC 2400
CTCCCGGGTT CAAGCGGTTC TCCTGCCTCA GCTTCCTGAA TAGCAGGAGG TTGTGTGTGC 2460
CACCATGCCC GGCTAATTTT GTATTTTTAG TAGAGATGGG GGTTTCACTA TGTTGGCCAG 2520
GCTGGTGTTA AACTTCTGAC CTCACAATCC ACCCGCCTCG GCCTCCCAAA GTGCTGGGAT 2580
TTCAGGCGTG AACCACCGTG CCTGGCCTGG 2610
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