| Tag | Content |
|---|
EnhancerAtlas ID | HS098-27990 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:41920420-41921550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr19:41920423-41920434 | TGGGTGTGGCC | - | 6.62 | | SNAI2 | MA0745.2 | chr19:41921199-41921209 | TGCACCTGTT | - | 6.02 | | ZNF263 | MA0528.1 | chr19:41920502-41920523 | GGAGCAGGAGCAGGTGGAAGA | + | 6.86 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_23546 | chr19:41920456-41921573 | Colon_Crypt_1 | | SE_42664 | chr19:41918772-41921696 | Lung | | SE_65911 | chr19:41918946-41923155 | Pancreatic_islets |
|
| | 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 |
| GH19I041414 | chr19 | 41920518 | 41921351 |
|
Enhancer Sequence | CTGTGGGTGT GGCCTGTGCA GGAGACCCTG TCTGCCTGGT GCAGTGATCC CCTGGCCCCT 60
CCTCAGGTGC TGTATCCTTC GGGGAGCAGG AGCAGGTGGA AGAACCTTGA CAGACCTGAG 120
TGCGGTGCAA GATTAGAGGG GCCCGGCAAG CCCAGATGAG TGAAAGGAAG GAAGGGTCAA 180
AGACCAGGAA TGAAGAAAAT CATTGAGCAG GAATGAGTGC CTGGGAGCGA AGGAGTGAGC 240
CCAGGGAGCA GTGAGTGGGG TCTTCCAGGG AGCTTGTTGG TGTGGGGCCC TGCATGGGGA 300
CTACCCTCAG AGTGTCAGCG AGCACTGATA GGGCCAGGAA GGCATATCTT AACCCTTTGT 360
CTTAGATGCT TGGGGCAAGT TGCTTAACTG CCCTGTGCCT CTGTTTCCTC ATTCGTAAGG 420
GGGATGGTAG CCCTTCCCAA GACAGCTGTT GAGGGCAGTC TTGGGGCAGT TGGCAAAGTG 480
CCCTCAGCAC AGAGTAAGCG CTCAGGGCCA GGGGTTGGTG TCATGATCGG GGACTCGCCC 540
TGGGACAGCC CTTCAGCAGG GCCAGACCAC GTGGCTGTCC AGAGCCCCCA TGGACCAGCA 600
TGGCTTGCAG CCTGCTCCTG GACTGTCTAC TGCTCACAGC TGGACCAGGC CCTTGGCCCC 660
ACATGCTCTA GGAGGGCAAA CGCCCTGTGG TGTTTGTCTA AGGTCTAGTG TCATCCGTGC 720
GGAAAAAGAT TTCCAGACAC CAGGCAGCAA GCTGGGCCCC CGCCAGCTGT GCTGAGCACT 780
GCACCTGTTT TTGCTGAAGG GTTCTCTTGT GAGGGCACCA GGCAGGACCG AGCAAGCCTC 840
ATGGGAATCA TGGGAGCCGC TGAGCTCTCC ACATGGGAGA GCTGGCCGCC TCTGCAAGAA 900
TGACTGTCCA GCACTGAGGG TCAGCAGAAG TGTCTGGGCA GCTGCAAATG GGACTCATGC 960
AGAGGCAGCA TGGTGCAGGG TAAGGAGTTG AGTCACATCC ACTCTAGACT TCACTTGGCA 1020
GGCCACTCAC CTTGGTGACG CTGTCTGTCG TCTGTGAAGT GAGAAGAGTG GTGTTCATCA 1080
TGATAGGTAG TGCCTCCCTG GGCTCTTGAC ACCAGAGTGC TGTTCTTTTT 1130
|
