| Tag | Content |
|---|
EnhancerAtlas ID | HS065-02240 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr17:47099560-47100610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr17:47100148-47100163 | TGACCTTTGACCTTA | - | 6.43 | | KLF5 | MA0599.1 | chr17:47099774-47099784 | GCCCCGCCCC | + | 6.02 | | NR2C2 | MA0504.1 | chr17:47100148-47100163 | TGACCTTTGACCTTA | - | 6.99 | | Nr2f6 | MA0677.1 | chr17:47100148-47100162 | TGACCTTTGACCTT | - | 8.12 | | Rxra | MA0512.2 | chr17:47100148-47100162 | TGACCTTTGACCTT | - | 7.82 | | ZNF263 | MA0528.1 | chr17:47099962-47099983 | CCCTCCTCCCCCTCCCTCTCC | - | 6.03 | | ZNF263 | MA0528.1 | chr17:47099959-47099980 | CTGCCCTCCTCCCCCTCCCTC | - | 6.18 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_28143 | chr17:47097531-47100459 | Fetal_Intestine | | SE_29263 | chr17:47098284-47100627 | Fetal_Intestine_Large | | SE_32734 | chr17:47098330-47101339 | H1 | | SE_67981 | chr17:47049476-47113351 | TC32 | | SE_68412 | chr17:47048796-47109684 | TC71 | | SE_68710 | chr17:47098054-47101902 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I049020 | chr17 | 47097577 | 47101136 |
|
Enhancer Sequence | ACTGCCCCAG CTCAGCCTAC ACCAGGCCTT CTCTAAGTGT TTGTGGAATG AATGAGACTG 60
GGACCAAGGG AAGGGAATAC GGGTTACAGT GATCAGAAAT GCCCCATGTG CTTTGAGGCC 120
TGAAAGAAAT TAGGTAGCAC CATATTTAAT AGAAACCGGG CCAAGGGCTT AAAAGACAAA 180
GGTTCTTCAC GGCCTCTGTG CCTCCCTGCC CCCCGCCCCG CCCCTCCCGC TGTTGTGTTT 240
TAATCAGGGC TGGGGGCTTT GTTGAAAGGA GGCAGCCTGG AGGGGCCTGG AGTGGGTTCC 300
CAGGGTGGGG TGTGTACCCT GGAGGGCTGG GTGAGTCCCT GCTGGTTGGG GGCAGGGGAG 360
GGCTGCCAGG ATGTCTTTTC TTTCATTGGT TGGGTGGCCC TGCCCTCCTC CCCCTCCCTC 420
TCCTGGAACA TTCCAGACAT TCCAGACGAT CTGCCTGCCA TTGCTTTCAG GATATGGATT 480
AACATCCTAG CAGAGATTTG ATTTCACCAC TGCCACCCTT CTCCCTTCCC CCATCCCCTC 540
CACGAAAGAA AGCCTCTAAA ACTGGGAGTT TGAAGTGCGA GGGAATTTTG ACCTTTGACC 600
TTAGATTGTA CTAAGGGACC ATCTTGAAAG AGCACACTTC AAACTGGGCC CCTAAACTGG 660
GGTTCCCTTA GGCCCTTACT GGTTTGAACT CCCAGGTAAG CCACCCCCAC CTCTCTGCCC 720
TTCATCCAGA CATCCAGAAG TGTTCCCTTG AGGGAGGTCC TGGGCCTGGG CCGAAGCAAT 780
ACCTGTTATA GGTGTTAAAC TAGGTCTGCG TTCTCAACCT TCCAATGGCA TGGCCATTTC 840
TTTTCCTCAT TTCTTCCGGC AGTTTTGCTT TCATTGTGAG GGCTTCTACA TTTTCAGTCT 900
GTCTAGTTGG TCATCGAATG AGTTCTAGGA AATTCCTCAC AAGGGTAGAT GTGGGGGTTC 960
CCTCTTGGCC AATGAATTGA ATCACAAAAA GGTGGTCTGA TGGCATCTGG GGACCTGGAA 1020
CTGGATTTGT ATCTTACTAT TTTGTCCTGC 1050
|
