| Tag | Content |
|---|
EnhancerAtlas ID | HS091-23820 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:33880780-33882200 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr19:33881456-33881467 | ATTGCACAATC | + | 6.32 | | CTCF | MA0139.1 | chr19:33881924-33881943 | GTGTGCCACCTTCTGGACA | - | 6.2 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_24617 | chr19:33880403-33881031 | Colon_Crypt_2 | | SE_24617 | chr19:33881414-33881913 | Colon_Crypt_2 | | SE_25205 | chr19:33878728-33881181 | Colon_Crypt_3 | | SE_25205 | chr19:33881227-33882626 | Colon_Crypt_3 | | SE_27838 | chr19:33878896-33886358 | Fetal_Intestine | | SE_28702 | chr19:33878791-33886507 | Fetal_Intestine_Large | | SE_52890 | chr19:33879155-33881099 | Small_Intestine | | SE_52890 | chr19:33881290-33884549 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I033388 | chr19 | 33878998 | 33889454 |
|
Enhancer Sequence | AGAACAGGGC GCAGGCGCCA TAAGAGAATG GGAAGGGCTG GGCCGGGTGG AGCGCAGAGC 60
CATGTGGGGA GGGCACGAGC CCCTGTGGCC CAGGAAGCGC AGCCTTCAGG GGTGGGGAGG 120
GGTCCTGCCC TCACCGCGCC CATGCTCGCC TCTGCCTGGG CACAGGGCTT GACAAGGCCT 180
CAACTTTTAT TGGGCTCCAA GCAGAGGAGC CCCAGATGTG TCTGCAGGCC TGAAATAAAA 240
CAAATGACTT TTATAGGAAA AGCCATATTT TTTCCACAAT GTTTATCTGT CAGAAGAATA 300
GACTCTGAGC ACAAAGAGGT GCTTACTGGA AAAGATGAAA ACAGTTTGCT GCCAATTTTT 360
GCTGGTGGAA AAAAAGCGCT TTGGCGACTA ATGAATAACG AACCTCAGCT AACAATGTCT 420
GGAAGGCCCA GCTCTTGGCT CCCTGCACAC AATGGGATGA ATAGACATTA GGAAATTAAA 480
ACTGATTTTG TTTCTCCAAA TTTAACTGTT TACACTTGAG GAAAAAAATA ATTGAATAAT 540
AATGCTTCTC TTAAGCAATT CCCCCCACTG CCCCCACCCT GCCAAAAAAT CATTCTTAGT 600
GCTTTCAAAA CACCCTGCAG CCAAGAGGCT GAGCCTTGTC TTGGCTAACT GGCTGGGGGG 660
CCCCAGGGCG TGCACGATTG CACAATCAGC CCCCTGCATT GGGCAGCCCG CCAAGGGCAG 720
GGATGGGAGC GCCCCAGCCG CCCAGCCGAG AGGCCGTAGC CACCTGCCCG GTTGGGCCTC 780
CCCAAGCCTC ACTTACCCTC TGGGTGGTCC TCTGAGGGCC GGGGAACCTT GTCTGGAGAT 840
GGCCCCCAGC CTCCCTTATC TGCCAACGGG CCCCAGAATG CCTGGGGATG AGGAGGCTGC 900
AGGGTCCCAG GTGTGCGGCC CAGGGGCCTG GGAGGAGAGG GCGAACCAGC GGCAGAGCAG 960
GGCTGCTCCG GGTTTGTGAG GGGCCAGGGT GAGTCGCCAG TGGGTGGGGC CTCATCAACT 1020
CCCCACGCCC CAGGTCTGAA TGAAGCCAGA GGCGGCAGGA CGTGAGGGGT GCCACGTAGC 1080
TCCATCACGA AGACCTGTCC TTAGCACCAC TGTCCTGTGG GGCCCCATGC ACCGTATCCT 1140
GACTGTGTGC CACCTTCTGG ACAGGTGACA CCTGGGCCCA GCAGGCAGAC AGCACCGCCT 1200
CTATGTCCAG TTCTGTGGAA TGCTCACAGA TGCACCCCTG TCTTGGCCAG GGTCCCGATT 1260
CCCCCCTCCT CATGGCCTCC GTATACCACA GGGAGCCATG GGGCCCATCC CTGCCATCCC 1320
AATACACGCC TGCTGCCTCC TAGAGTCCCA CCCTGCCCTG GGGGTCAGGC TCAGCGGCAG 1380
CTGATGGGCA GGCCACTCCG CCTGCCATGT CCACACTGAC 1420
|
