| Tag | Content |
|---|
EnhancerAtlas ID | HS034-10967 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr16:11783760-11784530 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr16:11783835-11783846 | ATATTTACATA | - | 6.62 | | ONECUT1 | MA0679.1 | chr16:11783826-11783840 | GAAAAATCAATATT | + | 6.76 | | ONECUT2 | MA0756.1 | chr16:11783826-11783840 | GAAAAATCAATATT | + | 6.75 | | ONECUT3 | MA0757.1 | chr16:11783826-11783840 | GAAAAATCAATATT | + | 6.92 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_10434 | chr16:11782497-11784584 | CD19_Primary | | SE_11208 | chr16:11762424-11786074 | CD20 | | SE_31676 | chr16:11783922-11784404 | Gastric | | SE_43514 | chr16:11771151-11787464 | MM1S | | SE_62988 | chr16:11758191-11785300 | Tonsil | | SE_67152 | chr16:11771151-11787464 | MM1S |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I011689 | chr16 | 11782172 | 11784710 |
|
Enhancer Sequence | TGACTGGTCA CAGGGTTCTT TTACACAGTG AGGAACTCTT GGATTTATAA TATGTAACTT 60
GATATAGAAA AATCAATATT TACATAAAGC CTTTTCACAA ATGTGTCTAA TGTAAGAAAC 120
AAGCTTCACC TAGATTTGAA AGAGGATGGC TAAAAAGACT CATATGTAGA AGCTCTGAGT 180
CTACTGTTGA GTTCATACTT TAAAACTTGA AATGAAAGGT TTCCTTCCCT ACCAAATTCC 240
TCCTTTCTCC ATTCGGCATA CACTGACCCT CCCTCCCGTT TCCAATGAGG CTGAACTAAC 300
GTGGCTTTTG AATTCTCACT TCATTGTGTG TAGTCAAGGG CATCAGCAAA TTCCTGGGAA 360
CAGGCCAGGG TGGGTCAGCC CAATGTTGCT GCCAAGTCCC AGGGGCAAGC TCTGGGTGCT 420
TTCTCATCAT GGAGCCTTAC TCCTCAAAAA GTGGGTTTTG CTGGTTTGCG ACTGACACTT 480
ATTTATTTGC ACTTTACACT TGTTACAGTG TAGGTACCCC AGGTCCCAGC AATATTACTC 540
AGTACATTAT GAAACAGCAG CAGAACAAAT TAGGTCTGGT GGCCTTGATC CTTAGACATT 600
TAAGCCTATG AGACAAAAAG GGAGGCAAGG CGGCTCTACT TCCTTCTTCA CTGCTCTCTT 660
TTTTTGGAGA CGGAGTCTTG CTCTGTCGCC CAGGCTGGAG TGCAGGGGCG CGATCTCTGC 720
TCACTGCAAG CTCTGCCTCC CAGGTTCACG ACATTCTCCT GCCTCAGCCT 770
|
