| Tag | Content |
|---|
EnhancerAtlas ID | HS050-69571 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:98938940-98941320 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr9:98939355-98939366 | AAATCACAGCC | + | 6.02 | | IRF1 | MA0050.2 | chr9:98939744-98939765 | AAAAAAAAAAAAAAAGTAAAG | - | 6.01 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_50729 | chr9:98939027-98940795 | Sigmoid_Colon |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I096176 | chr9 | 98939183 | 98940230 |
|
Enhancer Sequence | GTAGATGAGT CGCCATTCTC AAGACAAGTA TAAAATGCAA TTCAAATTCA CATCTACTGA 60
GTTTCCATAA TTATAAGATT TAAGTTATAA GATTTGCATA ATATTTATCG AATGTCTGCT 120
ATACACAGAG GACTGTGCAA AACATCTCTA AGGAAAGGAA GATGATCAAG ACATAGGTCT 180
TGATCTTCAG GGAACTTATC GGCTACCAGA GAAGAAAAAA TGTATGCACA AATAATATCA 240
AACTATGTCA GTATGTTCCT TAAGGGAGGT GCAGAGTTCA GAAGGTAGCA TATAGAGGGA 300
GGTTTAGGGG TGATACGTGG AGCCACTCTC ATTTGTGCCA GATCTTGACA AGTAGGAGGG 360
AATTTAGGGG AAGGAGCGAT GACACAAAGC CATGGAGTTT ATTGGTTAAA GCTGGAAATC 420
ACAGCCCACG GCCAAATCCA GCCAACAGAT GTGTTGTGTT TGGCCACAGC AATGTTTTTA 480
AAAAATTTGA ATCGGTCACC AGCATCTTAA AATTGAGATT TCACATACAA TTCTGGACCT 540
TGCAGCTTCT CTTTAAAAAC TCAGCTGTTG ACACTGGGTG CACATCCCCA CATAATCCTA 600
AGAGCCAGCT GGAGCTCCAC AGCAGCTGCT CGCCTAAGAC AGGGCACACA GCTCACCAGG 660
GCACTGTGAT CCCCACGCTG CCCGCCTCAG CCTTGTGAGT GTCCTGAGTC TCCTGCGGGA 720
GGCAGCCTTG TGACTCCTGA TTTAAAGTCT GAGGGTGGGT CAGACCAATG CTGGTAAAAG 780
TTTAACAACA GACACTCTCT TGAAAAAAAA AAAAAAAAAG TAAAGATCTG ATTGTAGCAT 840
TTGCCAATTT CTATTGTATA AATACTGCCA CCGTAGCCTA TTTCAAGCTC CCAACATTAG 900
GTCACTGAAA CTGGAGCTAG GGAAGAGATG CACGCAATTG GCTCTCACAG GCTGGTGAGA 960
GCCAGCCTCA GCACACTGCT CGGTCACATA GACCTGAGGG CAAATGCAGA CCCCCTAAGG 1020
AAGTTTCTTA CCTCCACATG CCAATGTCCT CCTGTATTAA CAAGGAGAAA TCGTTGCCTG 1080
CCTGCTAGTA CTATTGTGGG GTTTAAATAA TTTCCAGTTC ATCAGCTCAC CATTCAAATA 1140
GCCTCCTGTT TAATCCTTGC CCTGAGGTTT TTGTCAATGC TGCATTTTTT ATTTTTAAAG 1200
TTTAGATTTT TTTTTCCGCA TGTTTCTGTT ATTTCTAAAT AACATTTTGT TTTTGCCTTC 1260
TACAGGGCCG TGATGTAGGT ATTCCAGGCA TCCTGTTGCC TGTGTTCCTC CAGTGTGAGA 1320
TCTCTGGGCA TTGCCTCTGC ACACTATTTC AGACTGCTTG ATTTCCACGG CAATTAGAAG 1380
TTTTTCATGA GAAATTATCT TGGGAAAGAG GTTTTCAGCA GCAGCATTGT TGCCTCTGCT 1440
ACGACACATT GTAGGCACGC AGGTCTAACC CAAGTTTTTT ATTAATTTAT CAGCTCGGGC 1500
TTCCCACAGT GCCTGAGTAG TGTGGGCCCC CAACTGCAGG AGGGCAGCCT CTGCTTTACA 1560
TTTTCAGGAG GCTCTTCTTC TTCCCCAGCC CTGAATGGGC AACGCTTCTT TGTCTGAGCC 1620
AGGGAGTGGA CAGTTCTTAC AGACCCCGCC TCTTTGCAGG ACCCCCTTCC AGCTCCCCAC 1680
CGGCCTGGCG CCAAGGCCCT CGCCCCACGG TGCGCCCCTG GCTCCAGCCC TCTCCCTGAC 1740
TCTCAGTCCA GTCCTGCTCA CCATGCTGAC TTTGCTTCAG GGACCTGGGG ATTCCCTCTC 1800
TGACTTTTGA GTGCACTATG AATTTTGGGG TTAAAATTGT TACATTTGGG CAGCAGGAGG 1860
GGACTGGATG TCTGTATGGA ATGAAGAACA CAGCTCCTGG CACACAGGGG GACTCCACAA 1920
ACAGGGGACT GTCCTCTGGG AGCAGGAAGA GGCACAGCAC AGTCCGTTTA CAGGGATGTG 1980
GGGCCATGCC GGGCCACAGA AAAGGTGGGC GCCATCCAGG GCATGGGATG GGAAGGAGGC 2040
CGTGCTTGGG AGTTTAGAAG ATGGCCTCAG ACCAGGGACA TTGAGGAGTT CTGAGCAGAA 2100
GACTCCATGC AGAAGTTCTG CCTTTACAAT TTGATTCTGG AAGCAAAAGC AGGAAGGTTA 2160
ATTAGGAGCC TCTTGCCACA GTAAAAGGAA GGGGCCACGG GAGTCCGGGT TAAGGGACTT 2220
GGTGTGGGGC GAAAACAAGA GATGAGATGC AAGAAACACT GCTGGGTGAA ATCCGCTGCT 2280
CATAGGCCCC ATTGGCTGTG AGTGAGAGGC AGGACATCAA AAGCACCTAC TACTGGACTG 2340
TTAACAGGAG AACCGAGACA GAACATCAAG AACACAGGAA 2380
|
