| Tag | Content |
|---|
EnhancerAtlas ID | HS180-04440 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:211787840-211788490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:211787848-211787863 | TGAACTCCTGACCTC | - | 6.22 | | Nr5a2 | MA0505.1 | chr1:211788287-211788302 | GATTCCAAGGTCAGG | + | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28267 | chr1:211787832-211788720 | Fetal_Intestine | | SE_29189 | chr1:211786057-211788707 | Fetal_Intestine_Large | | SE_54270 | chr1:211787822-211788656 | Spleen |
|
| | 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 |
| GH01I211610 | chr1 | 211784144 | 211788437 |
|
Enhancer Sequence | GCTGGTTTTG AACTCCTGAC CTCCGGTGCT CCACCTGCCT CAGCTTCCCA AAGTGCTGGG 60
ATTACAGGCG TGAGCCACTG CACCCAGCCT CACAGTTTCT TTAAGGAAGT TAAAGGTCCT 120
CACTTTACTG ATGAGGAAAC TGAGGCTCAG AGGGGCTGGG CAGCCTGGGA AGTGGCAGCA 180
CCGTGCGTGG GTCTGCCTGC CTCTCAAGCC TACGCTGCCT CCAGGCTACA GGGCAGCCGG 240
GACTCCAGCC GCATCTCTGC CTCTAAGTCC ACCACACCCA CGGCCTTCCT GGCGAAGGAC 300
GGCCTTGTGT GCCCTGACTG AACACCTATC AGTCTATGGT ACCCGTTGTT ATCAGAACCA 360
GCAGAGTGAC CTCAGGGCAG ATCTTCCTAT CTCGCACATT ACACCTGTGC ACCTCCGTCC 420
TTCTGAAAGG AGACAGCCTG GCAGGCTGAT TCCAAGGTCA GGAGAGTGGA AGTTAAAAGA 480
ACCTAAAGGG AACACTTTTC AGTGGCCTAA AGGGGACACT TTCCTGCCAT CAAGCCCATG 540
GCCATGTGAG CAGAGCTTCC TGTCAGCCCC AGATTTGACT GCAGTGGCCT TAAAGGAAAC 600
AGACATAACA TCTACCTGCT AATTTCTATC ACATCACAAA AGTTCTGTGG 650
|
