| Tag | Content |
|---|
EnhancerAtlas ID | HS156-04818 |
Organism | Homo sapiens |
Tissue/cell | P493-6 |
Coordinate | chr16:70453390-70455490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr16:70453903-70453918 | TGACCATTTGACCCC | - | 6.6 | | RARA | MA0729.1 | chr16:70453900-70453918 | AACTGACCATTTGACCCC | - | 6.53 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_27776 | chr16:70448923-70457488 | Fetal_Intestine | | SE_28634 | chr16:70448899-70457647 | Fetal_Intestine_Large | | SE_32687 | chr16:70449734-70453680 | GM12878 | | SE_35582 | chr16:70450535-70453802 | HepG2 | | SE_39873 | chr16:70453030-70454522 | K562 | | SE_53222 | chr16:70450475-70455599 | Small_Intestine | | SE_54346 | chr16:70452045-70453868 | Spleen | | SE_59329 | chr16:70441356-70474175 | Ly3 | | SE_68952 | chr16:70451901-70453796 | H9 | | SE_68952 | chr16:70454711-70455820 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I070414 | chr16 | 70448014 | 70458303 |
|
Enhancer Sequence | CATAGGCACA AAGGCCCTCT GCAAACCAGA GGGCAGCGGC ACAGTGACCT GGCTGGCATA 60
CTGAAACAGG CTCAGCCCAA AGCTCCAACA CACAAGACAA GCTAAGCCCC TGAGAATGCT 120
GTGAGAGCTT CTGGGACATG AGGCCCTGGG TGCAGCAGCC TCGGGTCTCA GAGGCTTCCC 180
TGTCCCAGCC TGGCGGCCAG AGGTCAGAGC AGCTCGCTCG CCTCGCTAGT GCTGGCATCA 240
CACTCAAAGG TACAGGTGAA AACATGGTTC TTTCTCATCA TCAGCCCCAG TCATGGACCT 300
CGCCTCCTCC ACCGGGCTGG TATGACCTCT GCCTGTAATC TTTCAGTCCT CCTGCCCAGC 360
CAAGCTACCA AGGTGGGGTG TCCGCCAGAA CCACTGGGGC CAGGCAATAT GATGACAGCA 420
ACAGTCCAGG CTGCAGGTAT GGAGGCCTAC TTTGTACCAG GCAAATCCCT CCAAAGGGCT 480
CCTATGTTAT CAGTGGGGTA GGGACACCAC AACTGACCAT TTGACCCCCC CCTTCCCTTT 540
TTTTTTTTTT TTTTTTTGAG ATGAAGTTTT GCTCTTTCAC CCAAGCTAGA GTGAAATGGC 600
ATGATCTCGG TTCACTGCAA CCTCTGTCCC CGGGTTCAAA CTTCCATCAA CTAGGCCAAC 660
TTCTTATCAG TTTCTATTCT TGTGGCCCAG TGGGAGGATG GAACCAGGTG GGGAGACTTC 720
TATAGTTTCT GCCAAGATCA AATGTTGGAG AAAGCCTTTT GTATGGCAGT TCGTGGGCTA 780
AACTGGCCTG AGCAGCATGG CAAGAGGTAG GTCATATTAC AAGGCCTACA TGGAACAAGG 840
CTGCACTCCT AAAAGGTCCA GTCACATAGG TGCCAATCAC CTGGGAGACC TAGGGAAACA 900
GGCATCCCTC CCTCCGCCAC CACAGCCAAG AGCCCTGGGT AGAGAAGAGG GCAGAACAGA 960
GATCTGACTG CAGGGTGGTC AAGTAGTCTG GAGAGGATTC CTGGTGGCAT GGGTCCTACA 1020
AGACAACCTA GACAGTGGAC AAGCCAGCAC TAGGAGGCCA GAGAGCCTGG CGAAAGGGCC 1080
TGCAGACGTC TGCTGGCCTT GGAGGTGGTT ATCTCCTGGA AGGGGAATAA CAGGGCAGGG 1140
TCCGAAAGCT TTGGAAACAA ACCAGTAACT TGTTCTTTGT GAGCCAGGCT GTTTTTATTC 1200
TTTGCACGCC CTATCTTTAG CTTTCTTTTG TTCTCCTTTT ATATTTAGTA ATGTCTTTTG 1260
GAAAGGTCAG CCTGTGGCAG CTATGCTCAT GGAAACTCAA GGAAGGTGTT TGCATCCATG 1320
CTTCTACCAG AAGACTAAAA GGAAGCCATG TCCTCCCACC CAGCCCTCCA GAGTGAAGGT 1380
ATAGAAATGC AGAGTAAAAG ATGGAGGGAA CCAGAGGTGG GCCCCTTGCT CAGCTGCTGT 1440
GTCCTCTGGA CACTTCCTTT CCAACAGGGA CCCTGGAAGT TCCAGCTAGG AAGAGAGGTC 1500
ATTGTGAGCC CACGGCCAGC CTGGTGCCAT CTGGTAACTT CCAGCACCAA CCCTGCAGGT 1560
GGCTTTGGGA AGCATCGCTG TCCTGCACCC TGCTTTTCCC TGTCACTAAG GTTCAGCCCT 1620
GGGAGGTGGG CTGGGGAGGA CAGTGCCTGA GAGCCCAGCA CACACCTGCC TTCATGGTCC 1680
CGAGCTCCAG CTGAGCAGTC TTCCTCTTTC CTGAGGAGCC GATGACATGC TGTGACCTAC 1740
TCAGGCAGGG CCCCTGGTTG CTAGGGAATC AGTTCACCAC CTCTGGAAAG TGGCAATATC 1800
GCTGCTGTGA GTAGGCCCAA AGTGGGCCTT TCCCTGGCAC CGCCTCTGAG CCTTATCCCC 1860
GGGGTGAGAA AAACGAAGGT TGGGGGACGC CAAGGGCCCT CCTCGGTCCC TGCTGCCCAT 1920
CCTCAAGGAC TGACCTGCCC TCCTGGATCT GGCCTAAGCT GAGTTATAAG CTCCCTGCCA 1980
AGACAACATC CATCGTGCCA TGTACTACTG TTGTCAACTT TAGGGGGATG TGGAAAGGAA 2040
GGACGCACAG ACCTTGGTCC ATTACAGTGG ACCCCAGGGA GCTGTCTTTG TTGTCCAGCT 2100
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