| Tag | Content |
|---|
EnhancerAtlas ID | HS050-02365 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:54728120-54729600 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr1:54728559-54728573 | AAACACGCCCACTT | + | 6.05 | | SP8 | MA0747.1 | chr1:54728560-54728572 | AACACGCCCACT | + | 6.07 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_01019 | chr1:54728225-54729178 | Adrenal_Gland | | SE_29698 | chr1:54728490-54729572 | Fetal_Muscle | | SE_31383 | chr1:54728503-54729624 | Gastric | | SE_41585 | chr1:54728942-54729617 | LNCaP | | SE_52383 | chr1:54728026-54729643 | Small_Intestine | | SE_54182 | chr1:54728583-54729832 | Spleen | | SE_65414 | chr1:54728807-54729931 | Pancreatic_islets | | SE_68686 | chr1:54728431-54729703 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I054262 | chr1 | 54728027 | 54729931 |
|
Enhancer Sequence | GGCTGAAGGA CTTGGGAGAG CACCGAGATG CCGGGTGCTG ACCTCCTATG TGGCCAGCCA 60
GCCCCATGCT GGGGTCTGGA GGCACATCAG ACTTGTCCTG ACCCTGAGGA GCTGCCAGGC 120
TAAGGACAAA AACGATTACA CAGAGAGAAA TAAGCTTAAG TGTTGGCTTA ACCTGCCAGG 180
GGCTCCAAGA GAGGGTGATG CCTACCTCCC TCTCACTCCC AGACAGGTAA ACTGAGGCCC 240
AGTGTGGCCA CAGCATGTAG GCCTGGTACC CCCATGAGCC AACCGGAACT GGGATGAGAA 300
CTGGGGTCCA CTGACGGGTC AGAGCTCTTT CCACTGCACT GCACTGCCTC TGCAGGGTGA 360
TGGCAGCAGG ACCAAGCCCT GGGGTAGACC TCAACATGGG GGAAAATCCC CACTCCTGAA 420
TCTGGGAAAA GGAGGCAGGA AACACGCCCA CTTCCTGTCC AGCCTTCCAG CTGCCCTGGA 480
CCCTGTTAAT GGACTCGCTA TTCCATCTCA GCTGGCCCCA AGATCTCTGA GTGGAGACAA 540
CTAACTCCCG CAGTTTCTTG TTATTCTTTC TCCTGTAATT TCAGCACTGG GTAGTGTTCC 600
ATCCAGCAGC TCCTGAGAGC CACTTAGGCA GGGCCCAGGA GGCTCTGTTA TGGGTGTGAT 660
CGAGGCAAAC ACTGGGCCAC TTCACGAAAA CTCCGAAGTG TGGACACTGA TGGTTAGTGA 720
AAAAGCCTTT ACCCACACTG ACAGCGTGGG GAGCAGAGCA TTCCCACTGT AAAACGGATT 780
CAAGGACTCT GCGGAAAAGC ATTTCAGAAG CATCAGCAGG ACCCCCAGCC CTCCCGCACG 840
CTCCGGCTAA GTCCCTGCAC TTCATCTGAA GCCGTCCTGG AGAGGCGGGT TGTGGTGTGA 900
CAGGAAGCGC CCACATTATG CGGGCCTGGG ATCCAATCCC AGCTCCTCCG GTTCATTCGG 960
AGTCCAGTTT CCCAACGGCT CTGAGCCTCA CTGCCCTCAT AAAGGAAATG AGGACTATTC 1020
CACAAACACT GCAGGGCTGT GGCACAGCTG GCAGTGTGAG GCACACGGGG TCCCCAGTCC 1080
TGGTCCCCAT CCTCCTGCTC CTGTGGCCAC TCGCCTGCCC TTTACAAGGA AAGCAGGAGC 1140
TTGACGTCTG GCCTCATCTC ACCAGGTCTG CTGAAGGCCA CATATCCTTT TTCATGAAGG 1200
CTTTCCTGCT CCAGCCCTTC AAGTGCTCTC TAAACACAGA ACCTTTCCTT ACTCCATGTC 1260
TGGGGGTGCC ATGTGGACCC CTCCAGGCCA GGCCACTCAC CCCCACAGGT ACCTTGGGGC 1320
AGGGCCCAAA CAGAGCAGCA GGGCTGAGGC AGCAGGCGAC CACACTGCCA TGGGCAAGGG 1380
GCAAGACCCA GCAAGCCCCG GGGCAGGCAC ATCTAACACC TTGGGGCTCA TAGGAACCAG 1440
GAAGAAAAGT TAGTACCAAA AGGGTGACCA AGTTGGTCTT 1480
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