Tag | Content |
---|
EnhancerAtlas ID | HS146-15654 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chrX:64897550-64899310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chrX:64898226-64898237 | TCTTATCTCCC | + | 6.62 | RREB1 | MA0073.1 | chrX:64898333-64898353 | AGTGTGGGGGTGGGATGGGG | - | 6.63 | ZNF263 | MA0528.1 | chrX:64899155-64899176 | ACTTCCTTTACTCCCTCCCCC | - | 6.08 | ZNF263 | MA0528.1 | chrX:64898158-64898179 | GGAGGAGTGGGGAAGGAGAGA | + | 6.36 |
|
| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00139 | chrX:64886466-64903258 | Adipose_Nuclei | SE_02089 | chrX:64897579-64900039 | Aorta | SE_02753 | chrX:64897553-64900020 | Astrocytes | SE_09664 | chrX:64890814-64902905 | CD14 | SE_11087 | chrX:64886308-64928388 | CD20 | SE_18139 | chrX:64898300-64900134 | CD4p_CD25-_CD45ROp_Memory | SE_18347 | chrX:64886440-64902690 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19204 | chrX:64897769-64900153 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20433 | chrX:64897647-64898653 | CD56 | SE_20433 | chrX:64899001-64900003 | CD56 | SE_22452 | chrX:64897484-64900257 | CD8_primiary | SE_25993 | chrX:64895578-64900300 | Duodenum_Smooth_Muscle | SE_35030 | chrX:64896815-64900250 | HeLa | SE_36819 | chrX:64897315-64900200 | HMEC | SE_37199 | chrX:64895513-64900713 | HSMMtube | SE_38193 | chrX:64895655-64900447 | HUVEC | SE_40903 | chrX:64897492-64900105 | Left_Ventricle | SE_42391 | chrX:64896848-64900119 | Lung | SE_44510 | chrX:64897505-64900030 | NHDF-Ad | SE_45176 | chrX:64896875-64899450 | NHLF | SE_46435 | chrX:64896608-64899909 | Osteoblasts | SE_49242 | chrX:64897616-64899956 | Right_Atrium | SE_50614 | chrX:64897520-64899186 | Sigmoid_Colon | SE_52105 | chrX:64897619-64900022 | Skeletal_Muscle_Myoblast | SE_53097 | chrX:64897462-64900157 | Small_Intestine | SE_54259 | chrX:64897435-64900059 | Spleen | SE_54931 | chrX:64896590-64899672 | Stomach_Smooth_Muscle | SE_59928 | chrX:64886386-64926160 | Ly4 | SE_62795 | chrX:64886580-64927676 | Tonsil | SE_63895 | chrX:64897588-64900035 | HSMM |
|
| 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 |
GH0XI065676 | chrX | 64895866 | 64900092 |
|
Enhancer Sequence | GGAGGTTACA GTGAGCTGAG ATCACGCCAT TGCACTCCAG CCTGGGTGAC AAAGCAAGAC 60 TCTGTCTAAA AAAAAAGAAA AAAAAAAAGA AATATGTAAA TGGAAAAGAA CAAACCCCCC 120 TCCCAGGTTC CTTATTCCCC TTGGTGCCTG GGCCATTGTA GATCTAGCAT ATGCTTGGTG 180 GGGACATCTG CCATTTGCTT TAGGGTTACA CTACATCTTT CTACTTTGAG TGCTTGAAGA 240 GTTGCTCCAG CAGGGCCTGA TGTGGGCCTG GTGAAAATCT AGCCTAGTTG CCTTTCTGTC 300 TGCCATAGCC TGGGCATTTT CCTAAGGTTG GGAGTTTTTT TCCTTCTGGT CTTAGGCCAG 360 TTGCCAGAGG AAACCGATGA CTAAAGGCTT CCTCCCTGCA ACGTCAACTT CTGGAACCTT 420 TCCTGATGAT TCCTACCAGT CAAGTCTGCC TTATTTGGCT ATTTTCTCCC CCCTCAAGTT 480 ACTCCCTCTC CTTGCCACCC CACCTCAACT AGTCCTCTGT TCTCCTTTAG TACAGGGAAT 540 GCCTTCTTCA AGTTTATACA ATACCACCTG CAAACTTCTT TTCTTCTTGT TTAGAGTCCT 600 AATATAGGGG AGGAGTGGGG AAGGAGAGAG GAAGATGGGA GAGCTCTGGA ATGACTGTGA 660 TTTCTCCACC CTGCTTTCTT ATCTCCCTTT ATCCTCTTGG CACTGCCTGG TCACTCCTCT 720 ACAGCTTCTT ACCTAGATCT CTGACAGCCT AGGAGTGGTC TCGATTGGCC TAAAGAGGTT 780 CAGAGTGTGG GGGTGGGATG GGGCTAGGGC TTTCAGCATT TGAAACTATT TCTTTGGAGC 840 AGGTAAAGCC TTCCAGTTGG TAAGTCTAGT TCTTTAAGTA TGCCTGTTGT ATGCCTAGCC 900 TTCTCACTTG GCTTTCCTGG GTGGGCTGAG TCTAAGTTCC CTCTACCTCC CCTTCCCAGT 960 CCTGAGCTGT CTAACTTTAG GTTAGAAGAG CTGAGCTTTT GACACTTACA GCTTGGGGCA 1020 CTTGTCTGGG TGTCTTTAAA AATACCTTTT AGTAAAAAAT GGTACAATGG AAAGAAGAGT 1080 GAGATATTTG GTTTTTAATC TCTGCCTGTG TGACCTTGGG CAAGTCACTT TTATGAGGCT 1140 TAATTTTCTT ATCTACAAAA TAGAGACATT GGCTTTTTCT GACATTCTGA TTATTTGTGC 1200 CCAGTCTTTA AGAGGCTAGG AAAGGGGTCT TGGAAAGCGT GTAGCAGAGC AGAGTGGTGA 1260 CTTTTCGGAG AAGCTTCCTT TTCCCATTTA GAATGGCATT GAGTGTGTCA TTTTCTCCTC 1320 TGGCTATCAA CATGTAAGCA GCCCCCTCTA TTTCAGTGAG CTCTGCTCTG GGATATACTG 1380 AATCTACCTA CCAGAGAGCT CACTGTGGAG ATTCTGGCTT GGAGAGACAA CTGTTGACTA 1440 CATGCCTTGG GTGGGGTCTT GGAGTCCAGC CTGCAGACTA CAGTTGCTGG CTATTTTTGG 1500 TCATCTGTGA CTCAGGAAGA ATAGAAGACC CTTGGATTGG TCATTGTTCC ATCAGGGAAA 1560 GGGAAGACAA AGAAACAAGC TAAAACTGAG GACATATGAG ATTTCACTTC CTTTACTCCC 1620 TCCCCCACAA CATCCCTTTT TGTAGGGCTA TGAAATTGCT TTTGACTGAG TCTTAAATTG 1680 CTAAGCTCCC TTTCCCCTTC CTCTATCTGA ATCATTGTTG ACTATGTTGC CCTTGGACGG 1740 GGAGAGCTAG GTGATATGGG 1760
|