Tag | Content |
---|
EnhancerAtlas ID | HS059-19892 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr17:47099840-47100580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr17:47100148-47100163 | TGACCTTTGACCTTA | - | 6.43 | 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 | AGGGGCCTGG AGTGGGTTCC CAGGGTGGGG TGTGTACCCT GGAGGGCTGG GTGAGTCCCT 60 GCTGGTTGGG GGCAGGGGAG GGCTGCCAGG ATGTCTTTTC TTTCATTGGT TGGGTGGCCC 120 TGCCCTCCTC CCCCTCCCTC TCCTGGAACA TTCCAGACAT TCCAGACGAT CTGCCTGCCA 180 TTGCTTTCAG GATATGGATT AACATCCTAG CAGAGATTTG ATTTCACCAC TGCCACCCTT 240 CTCCCTTCCC CCATCCCCTC CACGAAAGAA AGCCTCTAAA ACTGGGAGTT TGAAGTGCGA 300 GGGAATTTTG ACCTTTGACC TTAGATTGTA CTAAGGGACC ATCTTGAAAG AGCACACTTC 360 AAACTGGGCC CCTAAACTGG GGTTCCCTTA GGCCCTTACT GGTTTGAACT CCCAGGTAAG 420 CCACCCCCAC CTCTCTGCCC TTCATCCAGA CATCCAGAAG TGTTCCCTTG AGGGAGGTCC 480 TGGGCCTGGG CCGAAGCAAT ACCTGTTATA GGTGTTAAAC TAGGTCTGCG TTCTCAACCT 540 TCCAATGGCA TGGCCATTTC TTTTCCTCAT TTCTTCCGGC AGTTTTGCTT TCATTGTGAG 600 GGCTTCTACA TTTTCAGTCT GTCTAGTTGG TCATCGAATG AGTTCTAGGA AATTCCTCAC 660 AAGGGTAGAT GTGGGGGTTC CCTCTTGGCC AATGAATTGA ATCACAAAAA GGTGGTCTGA 720 TGGCATCTGG GGACCTGGAA 740
|