| Tag | Content |
|---|
EnhancerAtlas ID | HS068-03796 |
Organism | Homo sapiens |
Tissue/cell | GM18526 |
Coordinate | chr22:39842140-39843320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| YY1 | MA0095.2 | chr22:39842145-39842157 | GCAGCCATCTTG | - | 6.74 | | Zfx | MA0146.2 | chr22:39842500-39842514 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_27680 | chr22:39841486-39843367 | Fetal_Intestine | | SE_28597 | chr22:39841614-39843289 | Fetal_Intestine_Large | | SE_32335 | chr22:39841888-39843460 | Gastric | | SE_33664 | chr22:39839897-39843283 | H2171 | | SE_43884 | chr22:39840381-39845549 | MM1S | | SE_52444 | chr22:39841074-39843520 | Small_Intestine | | SE_54198 | chr22:39841803-39843269 | Spleen | | SE_58479 | chr22:39830959-39870572 | Ly1 | | SE_58827 | chr22:39832463-39870704 | Ly3 | | SE_59756 | chr22:39832313-39870994 | Ly4 | | SE_60418 | chr22:39832202-39869380 | DHL6 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I039445 | chr22 | 39841062 | 39845210 |
|
Enhancer Sequence | ACCCTGCAGC CATCTTGGCA GACATCTCCC ACCCAAGGAC CCCAAGCCTC AGAGCCGTCC 60
TTAACTGCTG GCAGCCTCCA GTGGGGCAGG GCAGCAGAGT GTATGGTGAT CCCCATGCTT 120
GCAGAAGAGG CCCAGGAGGC TCGAGGCCCA GCTGGGGGTG AGTAGAGGAG GATAAGCGGG 180
CTCTGGACAG GCCCCAGCGT AACCAAAGGC CATTTCCTCC AGAGGCCCCG GCTCTGTCCC 240
CGTCCCTGAG GGTGTTTTCC CGGGAATGAG CTGGGCCTGC TCCTCCTGCA GGTGATAACA 300
CTTGGCCCTG CCTGGGGTTT CCGAAAGGCG GAGGGCGCCA CACAGCAGCC GCTCCCTGGC 360
CCCGCCTCGG CCTCACAGAC TCTGGAGTGC AGCAAATGTC CCCAGACAGT GATGTTCACT 420
GAGGGTAGCA GGGGGGAAAC CAGGGTGGAT CTTTCCTCTC CTCCAACCCC TAGAGGCCTC 480
GTGAACCTTT CAGTGGCCTC CCAGCACAGG TGCTGCCACT CATTAGCTGC CTGATCTTGG 540
GAAAGTTAAC TTCACTGCTT CATGCCTGTT TCCTTATCTG AAAAATGGGG AGAAAGGAAG 600
GGCAGACACG ATTGCTCTGT GCCAGGCCCC GTTCTAAGCA CTTTGCATCT AGCAACTCAT 660
GCAAGCCTCC CAACAGCCCT GTCAGGCGGG GTCTGTTATG ACATTCCTCA CTTTACAGAT 720
GAGGAAATGA AGGCACAGAG AGGGCAAACA AGTTGCCTGA GGTCACACAG TGAGTCAGTG 780
AATCTCGGAG TTGGGCCCAG GTAGCCCAGG TCTGTCTTGT TAGCTGCCAT GCCCAACATC 840
ACGGCCTGGC GTGACAATGC AGGATGATGC CAGCCCGTGG TCAGTGATGT GGGTTTGCTT 900
CTGTGGTTAT CATCCCCGTG CTCTTTCCGG AGCCCGAACT GCACCTGCTC CGCTAGTGCC 960
TGTGCTCCGC CTCCTATTCC TTCCCTTTTC TATACCATAG TGTGGCTGAG GTTGTTTTAA 1020
ACCTGAATTT GTTTGAGCCC CTGAGCTTTC TAGTTGCAGT TCATTGCACT TCGCAGAGCA 1080
ACTGGCAGGA AGTGTGTGTG GTGGCCAGAG CTCTCGCCGC AGATGCAGGC CGTGTTAACG 1140
GAGCGCAGGG CAGCCAAGGC AGGTGAGAGA CCCTTTGTGT 1180
|
