| Tag | Content |
|---|
EnhancerAtlas ID | HS048-02473 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:156441120-156442390 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:156441141-156441156 | TGAACTCCTGACCTC | - | 6.22 | | TCF3 | MA0522.2 | chr1:156441618-156441628 | AACACCTGCT | + | 6.02 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_00337 | chr1:156441142-156442331 | Adipose_Nuclei | | SE_00902 | chr1:156441144-156442354 | Adrenal_Gland | | SE_01624 | chr1:156441200-156442527 | Aorta | | SE_02937 | chr1:156441219-156442272 | Bladder | | SE_03183 | chr1:156441626-156442087 | Brain_Angular_Gyrus | | SE_04925 | chr1:156440984-156442573 | Brain_Cingulate_Gyrus | | SE_05851 | chr1:156440769-156442691 | Brain_Hippocampus_Middle | | SE_06826 | chr1:156441161-156442351 | Brain_Hippocampus_Middle_150 | | SE_07824 | chr1:156441020-156442361 | Brain_Inferior_Temporal_Lobe | | SE_09328 | chr1:156441246-156442393 | CD14 | | SE_25856 | chr1:156440987-156442515 | Duodenum_Smooth_Muscle | | SE_26648 | chr1:156441198-156442347 | Esophagus | | SE_31445 | chr1:156440531-156444229 | Gastric | | SE_33523 | chr1:156440956-156442695 | H2171 | | SE_40614 | chr1:156440317-156442474 | Left_Ventricle | | SE_41764 | chr1:156441137-156442359 | LNCaP | | SE_42136 | chr1:156440965-156442533 | Lung | | SE_46671 | chr1:156441270-156441527 | Ovary | | SE_46671 | chr1:156441544-156441972 | Ovary | | SE_48054 | chr1:156440640-156442473 | Psoas_Muscle | | SE_48580 | chr1:156441106-156442480 | Right_Atrium | | SE_50090 | chr1:156439528-156442465 | Sigmoid_Colon | | SE_51078 | chr1:156440989-156452153 | Skeletal_Muscle | | SE_52473 | chr1:156441114-156442385 | Small_Intestine | | SE_54540 | chr1:156441149-156442434 | Stomach_Smooth_Muscle | | SE_65297 | chr1:156440754-156442837 | 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 |
| GH01I156471 | chr1 | 156440921 | 156442394 |
|
Enhancer Sequence | CCACGTTGGT CAGGCTGGTC TTGAACTCCT GACCTCGTGA TCTGCCCACC CTGGCCTCCC 60
AATATGCTGG GATTACAGGT GTGAGCCACC GCGCCCGGCC AGAATCAACT ATTTCTAACA 120
CTTGTACAAA CTAGGAAGCC AAGCCCAGAA CAGTACAGTG CCTTGCCCAA GGCCCCTCAG 180
TGAGTGAGTG ATGGAGACTA GCTCCCAGCC CTGCACTGTT CCACCAGATT CCAGCCCTAT 240
CTACTACTGG GAGGCTTGGC TCCCCAAGGA GGACCATGGC CCAAGGCCAC CTGGCAGCCT 300
ACTGGTCTGC TCCCAGAGCC ACCACAGCCA GGCCTCTGCG GCCAGTGTCA ACAAGGGGCC 360
AGGCCCTCAC ATGAGGCATT ACCATAGCCC GATTACCCCC AGCCGGAACT TGAACTGCAG 420
CCAAGGACTG TAAACAGTGA ACAACTAAAC AGCAATGTGT TCACTGGGGT TTTGTTTACA 480
CACCTAGGGT CACCTGAAAA CACCTGCTGT TTAAACTGAG ATCTGCTTAG CTGCTCCTGT 540
AACAAGAGGA AAGGGAGCCT GTGGTCTCTG AGAGGAGATG AGAAATCTCA CACACTTCCC 600
AGCAGGGCTC CAAGGGCGGC CCAGGGGCAG AAACTGCTTT CATGCCAGAG TGACAGATGA 660
GAATCTTTAA GTCTAGCCTT CCTGAGTGCC TGTCCCAGGT TGGCTGACAC CAACTAACTT 720
TCCTCCTGCT TCACAAAAGA CTGTGGGCCC AACAAGATGG CAGAAAAACA GAAAACCACC 780
CTCACAGAGT ACCTGATAAA CAGCTCCAGA AAAGTGGTCT AAAAAGTGGT CTGAGCTGCC 840
CTCCGCCAAC TGTCCCTGTC CCCAGGCCAC CCCACCCTCA GGGCTGGTTT TTCTGGTTGG 900
GCCCCAGAGG CCCAGTGGCA GGGCTGGAAA AGCCTCATAG ACCTCCTGTC TACCCACTCC 960
TCTTACAGAT GGGGAGACGG GCCCACAGCG TGTGTCTTCT GAAGCAGCCA TCTGTGAAGT 1020
TGCCAGGACA TCGTAGCCTG GGGCTGGGCA CACACATGGG TGCACATGCA AGGGAGAAGG 1080
GGCTCAAAGA CACCTGGGTG GTAACTACAC ACAGACACAC AAGCCAGAGT CTGGTCCCTC 1140
AACATGAGGC GGTCCCTCCA GCTCTCTTAA CCTGCCACGA GGGGCTTTCC TACACAGAGG 1200
GCTGGGTTCT GGATTTTTCT TTTTTTTCCC TTTTTTTGAG ACAAAAGTCT CGCTCTGTTG 1260
CCCAGGCTGG 1270
|
