| Tag | Content |
|---|
EnhancerAtlas ID | HS054-01278 |
Organism | Homo sapiens |
Tissue/cell | FT246 |
Coordinate | chr11:1145790-1148500 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chr11:1146831-1146842 | CCCACCTGCCC | + | 6.14 | | ZNF263 | MA0528.1 | chr11:1146306-1146327 | ACCCTCTTCACTCCCTCCTCC | - | 6.59 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH11I001154 | chr11 | 1146311 | 1146512 | | GH11I001153 | chr11 | 1147450 | 1148462 | | GH11I001152 | chr11 | 1146579 | 1147140 |
|
Enhancer Sequence | ACGCCACCCC CCGCCTGGAA GGGAAGATGT CTGCTCCACA GAGCCCTGGG GTCCCCTGTG 60
GGCAGGGTGT GTGGAGCTGC CCTCCCCTGG TCTCCCCAGG ACAGACCCCC ACCCTCCACC 120
CCAGGTGCCT TAGGGTAGGC GTGGCCTCCC CAGGTCCTGC CAGCCAGAGC CAGGCTGACC 180
CCAGCGGCCC TGCAGGTCAC CTCCTAGGGG CTGTGCCCGG AAACTGGGAT GGAAGCGACA 240
GGCTGGGGGC AGAGTGTGAG CCCAGCCCAG GGCTTGCGAT GTTGAAACCA GTGCTTCCCT 300
CCCCTGCTCA CCTGGCCAGT AACCACCGGG CTGGGGTGTC CTGGCTGGGC TCAGGCCGGG 360
CTGGGGGCCT CTCCTGATGC TGCTGGAGGG CAGACTGGGC CAGGTGCCCC CAACAGTGTG 420
CGCTCGGCCT GGTGGGGCTG AGAAACCTGG AACATACACA CCTGTGGGGG TGTCTAAGGG 480
GCTCCCAGGG AGTTCTGGGG GGTCCTGGGG AGCAGGACCC TCTTCACTCC CTCCTCCAGG 540
GGAAGTGGCC CTGGGGCACC CCCGGCTGTT CCCCCAGCTC TGTGGGGCCG AAGCCATCCA 600
CAGGGGGCTT TCCCCACCGG ATGTGGTGCG GGCCGTGGTT AATCTCACTT GAGTTAGTCA 660
CCCAGGACAA ACAGCTAACC GACACAATTC CTCCCAAGTC CAGGGGGCCG GAGGCGGGGT 720
CAGCACCTGG CGGCAGGAGA CAGTGCTGCC CTGGGATGTG GCCGGGCCTC CCTCCATTCC 780
CAATCCTGTT GTCTCTGTGG CAATACCTGG CTGGGAGCTC CTATCAGGCC CGTGACCCCC 840
GCCCTTTCTC CAGTGCCCTC CTGTCTGCAT TCACCTGTCA GATCCCGAGG AGAGAGGGGC 900
ACTGGCGGCC GCCCAGGACC AGAGCTGTGG GGCCTCCCGC ACCAGAGTGC AGTGAAGGTT 960
TGTGGGCTGC GGTCCCGGCG GAGCCCACGT GCCACCCCCA TGCACAGCTT TCCTCCTGCA 1020
CATCCCACAG AAGCAAAAGC TCCCACCTGC CCGGCACTGT CCCCGCCCTG GGGACCCTCC 1080
TGCAAACACT TTCCAGATGA CAGGCAGCTG CTGGTCCCAG GCACACACCT TCCCTGAAGG 1140
TGCCTCTCAC CTGAGGGTGC AGGTTCAAGT CAGGAGGGTG GACTCCTGCC CGGTGGGGTC 1200
ATCACCCTTC TCAGGGGCTG AGGCAGGGTC TGCTTTAGGG GTTGCGCCTG CTTTTCAGAC 1260
ACCGGCCCCC AGGCCCCTGC TGCAGCCCCA CCCGGACCGC ATGCGCAGCC GTGCCCGCTA 1320
AGTGGTCGGC GCTGCGGGCA GGGTGGCCGG GGCATCAGGG TTCCGAGATG CAAGTGCTGG 1380
GCTTGGCTAC CACGGGGGGT CGGGAGCTCA CGGGGGAAGA GTGATCCTGA TTTTGAGGCC 1440
AAGTCGCTGG TCTTACACCT GTCCTGGCTG CCGGTCTCAG AGCTGACACC GGCCCCAGGC 1500
TGGGGGAAGG TATCCAGCCG GCCTGGCCAG GGCCCCTGCT GGGAGGCAGC AGGAGGAGTT 1560
ATTGTGCTGG ATGGGGGTTG GGAGCTGAGG GGACTGGAGA TGGCATGGAG CCCTCCGGTG 1620
GGTGGGACTC CCGGGCATAT GCTGAGAGCT TTAGGCCTCA GGGAGGGTTC CCAGGAGGCA 1680
GGTGGCTGCG CCACGGCTCG GCCAGCCCTG CCTGCACCCT CTGAGAGCCC CCAGCAAGGC 1740
TGCAGTGACC ACCTCAGATT CCCCTCTGAG GCCTGTGGCG TGGCCGGGAC CTCACTGCCC 1800
CTGGGGACAC ACAGAAAATG CCCACAGAGC TCAGAAACAA GGCCCAGTGG GTTTTCTGGA 1860
AAGTTCTGGG TGTGTGGAGC CTGGGGCTGT AGGCTCTGGA ACTGTAGGCA CTGGCTTCAG 1920
GCCTCCTGAG GCCTCGGCCT GGTGGGGTTT TCATGGGACC AGGTGGTCAG CCCGTGGCCC 1980
ATGCCCAGGG GTTTTGGGTG CCTGAGCCCA GGCCCCAAGA GGAAGCCCAG CACAGCCAGG 2040
GGTCACCAAC ACTGGTGGGG GGAAGTCACC CCAGCTGGAC CCCAGCAGCG GCCCTGGGTG 2100
ACGTCTGGCT GAGGGAGGAG AAAGCTGTGG CTGGGGCGGC AAGGCCTGGG TGGCCAGTTG 2160
GCCAGGTGCC CCGGGGCTTG GCCCAGCCTC AGACACGCAG GGGGCACTCC CCTCTGAGGG 2220
CCACGCTGGT GACTCAGACT GTTCAGAGGT CACGGTATGG ACTGGGCCAG TGACTCAGGC 2280
CTGTCCTCTG TTGGGGGCTG GACACTGACT CACCCACTGC CTCCTGTCTA TCTGAGGGCG 2340
TAAGGAGGGC AGGCCTTCAG GCACTCACAT GCGGCCCTGG CCAGGGTCCC GGTCACACCT 2400
GCAGACCCTC AAGCCCTTCC CTATGCCCCA CTGACATAAC CACCTGGCCC TGGGATCTGG 2460
TCCCACCGCG GGGCCCATTG TCCACTACCA GGACCCTCCT CTGCCTTCAT CAGCACCAGG 2520
CGACCTGGTG TCCACTCCTG GGCCAGGGCA GGGGAACCCT GGCTACACCT GGTCGAGTCA 2580
GACCTCCTGA AGCACCAGTG GCTGGGGTGG TCCACCCTAA CCCTGTCAGC CGCTCAGCCT 2640
TAAATGTGAT CACTCGCTCA GTCAGTCGCC ACCCACTCAC TCACTCACCC ACTCACTTAT 2700
TCACTCACTC 2710
|
