| Tag | Content |
|---|
EnhancerAtlas ID | HS154-06373 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr14:55573490-55575930 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr14:55575108-55575119 | GATGAGTCACC | - | 6.32 | | JUND | MA0491.1 | chr14:55575108-55575119 | GATGAGTCACC | - | 6.62 | | ZNF263 | MA0528.1 | chr14:55575036-55575057 | GGAGGAGGGCGAGGGGAGAGG | + | 7.74 |
|
| | Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
| SE_00244 | chr14:55563236-55576350 | Adipose_Nuclei | | SE_00820 | chr14:55574748-55575102 | Adipose_Tissue | | SE_02600 | chr14:55573844-55576160 | Astrocytes | | SE_09388 | chr14:55568067-55576360 | CD14 | | SE_23110 | chr14:55574129-55575416 | Colon_Crypt_1 | | SE_23790 | chr14:55574297-55574562 | Colon_Crypt_2 | | SE_23790 | chr14:55574594-55575269 | Colon_Crypt_2 | | SE_24786 | chr14:55574109-55575428 | Colon_Crypt_3 | | SE_26013 | chr14:55573672-55575878 | Duodenum_Smooth_Muscle | | SE_26711 | chr14:55573567-55575917 | Esophagus | | SE_27630 | chr14:55573899-55576071 | Fetal_Intestine | | SE_28543 | chr14:55573873-55576230 | Fetal_Intestine_Large | | SE_31668 | chr14:55574018-55575868 | Gastric | | SE_33558 | chr14:55573897-55579764 | H2171 | | SE_34039 | chr14:55574107-55575498 | HCC1954 | | SE_34802 | chr14:55573592-55576155 | HeLa | | SE_36310 | chr14:55573891-55575863 | HMEC | | SE_37768 | chr14:55573433-55575974 | HSMMtube | | SE_41170 | chr14:55573962-55575665 | Left_Ventricle | | SE_42472 | chr14:55573658-55575611 | Lung | | SE_44570 | chr14:55573874-55576148 | NHDF-Ad | | SE_45117 | chr14:55573558-55575933 | NHLF | | SE_46036 | chr14:55573692-55576091 | Osteoblasts | | SE_46880 | chr14:55574151-55574573 | Ovary | | SE_46880 | chr14:55574627-55575401 | Ovary | | SE_49010 | chr14:55574074-55575920 | Right_Atrium | | SE_50181 | chr14:55574075-55575919 | Sigmoid_Colon | | SE_52430 | chr14:55573656-55575984 | Small_Intestine | | SE_56717 | chr14:55573869-55576081 | u87 | | SE_57551 | chr14:55574279-55575356 | VACO_503 | | SE_64542 | chr14:55574036-55575714 | NHEK | | SE_66903 | chr14:55573897-55579764 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 55574264 | 55575347 | | chr14 | 55574465 | 55575376 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I055097 | chr14 | 55563775 | 55576469 |
|
Enhancer Sequence | TTGGTGTTCA TCAAAATGGT AATTTTTCTC ATAGATTGAC TTTATGAGAA GTGAATGCTA 60
AATGAATTTT AACTTAAATG TAGATTCATA AATTATTTCT TTTGTGTTTT TATCTTTTAT 120
TGTTTTTTGA GACAGAGTCT CACTCTGTTG CCCAGGCTGG AGTACAGTGG CTTGATCTCG 180
GCTCACTACA ACCTCCACCT CCTGGTTCAA GTGATTGTCC TGTCTCACCC TCCCCAGTAA 240
CTGGGATTAC AGGCGCCCAC CACCACACCC AGGTAATTCT TGTGTTTTTG TAGAGGTGGG 300
GTCTCGCCAT GTTGTCCAGG CCGGTCTGGA ACTCCTGGCC TCAAGCGATC TGCCCGCCTC 360
AGCCTCCCAA AGTGCTGGGG TTACAGGCGT GAGCCACTGC GCCCGGCCTC CTTGGTATTT 420
TTATGTCTAT TTTTTTAGAT GGAGTCTCGC TCTGTCCCCC AGGCTGGAGT GCAGTGGCGC 480
GATCAGCTCA CTGCAACCTC CACCTCGCGG GTTCAAGCAA TTCTCCTGCC TCAGCCTCCT 540
GAGTAGCTGG GATTACAGAC GTCCATCAAC ACGCCCAGCT AATTTTTGTA TTTTTAGTAG 600
AGATAGGGTT TCACCATGTT GGCCAGGCTG GTCTTGAACT GCCTACCTCA GGTGATCCAC 660
CCACCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCGTAAG CCACCTGCGC CTGGCCGGTA 720
TTTTTAAATT AGAGTTCTTC TAAGATTTAT CTGAAAAAGT TACACTACTA AAAAATTTGC 780
AACCCACACC CAAGGACATA ATTTGTCTGG GCATAGAGAC TTGATGGCAC TTCAAGTAGC 840
TGGATGAGCT TCTCTTAACA TGCGATTTCT CTCAGGTTTA CATTCTTCTT GACTGCCCTT 900
GTTCCTTTCC TATTCTATTT GAAGCAAAAT GGTTAACGTT CTTCCACTTT CACCAGGACA 960
GCCCTATTTG CCCCTTCCTT GTCCTTGTTA GCCTGGTTTT ATAAAGCCTC TTTTGCAGGG 1020
GTCGGAACAG TTAATAGCAT TGGGGATTGT CGCTTGTTCC CTGTAGATGA AAAGTATTTT 1080
TCTATTGTTT AAAAAAAAAT CGAGGTCATT CTCCAAAGTA ATTTCCTGAA ATAAAGCGTG 1140
GGAGGAAGTC ATGGGCATGA GGATGAGTCA TCAGGCAGCA GCACGAGGCT GCAGGCGTGA 1200
GCTGGGGAGC CCTGGCTCAG TCCTCCGCAG GCTTGGATCC CTGAGCGGAG CAGGCCACTG 1260
GGGCCTTCTG CCGTGAGAAG AGACCTACTG AGAGGCGGGG AGTGGGGGTG GGAGTGGTTG 1320
CTTCTGACCT GTAGGACAGT GGTCAGCGTG GGCGGGTGGA GGCACAGGAG AAGGCCGACA 1380
GGCCCTGGGT CCTAGGGCCA CTCAGCTGCT GGAAAATGAA GTTCAGAGTT GTTTGGACTG 1440
TCTGAAGTAG GATAGAACCA GCCTTAGCCC TAGTTAGGTA ACACATGGCA GAGGCACCTG 1500
AGCAAAGACG TGAGCTGGAC CATGGGCTTC CTGGCAGGAC TTCCACGGAG GAGGGCGAGG 1560
GGAGAGGAGC AAGGGAGCAG AAGGCAGCTT GCCGTCCACG AAGCCTCCTG AGGCCCCAGA 1620
TGAGTCACCA GACAACAGCC TGTCTACTTA AAGCAACTGC TGGGCAACTG CTGAGTAGAA 1680
CAGTCCCTAA CCACATGAAC ACTGGGGAGG AGGTTCTGAA AGACGCTGCT GGGTGCAAGG 1740
TCCCTAACTA GGGTAATCCA ATTTCACTCC AGGCTAACAT GAGAAATTAT GACTCCAGCA 1800
GCCAATCCTG TGGGCCGTGA GAGAGTGGGA GAGGGATTTT CCAGATATAA GTCCCACTAG 1860
AGCTTCTTTT TTTTTTTTTT TTTTGATACG GAGTCTCACT CTGTTATCCA CGCTGGAGTG 1920
CAGTGGCACC ATCTCGGCTC ACTGCAAGCT CCGCCTCCCG GGTTCAAGCG ATTCTGTTGC 1980
CCCAGCCTCC TGAGCAGATG GGACTACAGA TGTGCACCAC CATGCCCAGC TAATTTTTGT 2040
ATTTTTAGTA GAGACAGGGT TTCACTATGT CGGCCAGGCT GGTCTCGAAC TCCTGACCTC 2100
ATGATTCTCC TGCCTTGGCC TCCTAAAGTG TTGGGATCAC TGGCATAAGC CACAGCTTCC 2160
GGCTGAGTCC CACTAGAGCT TCTAAGAAGA AATTAGGGAA GCAGGATTAT GAGAGGCCTG 2220
GTCCCACTCA CAGTGTGCGA CATCACTGAT GACTATGCTT GGTTACCTGC CTTGTTATTT 2280
GCTACCTTTG TTATTGTCTA TTTCTTGGTA ATTAGTAGTA CACTATAGTG ATTAGGAGTG 2340
ATCAAGAAGA TGCCTGGCTT CATATTCCAA CTTTGTCGTT TACTAACTGT GAACTTGGCC 2400
GAGTTTTTTT TTTTTTGCTT GTTTGTTTTG TTTTGAGACA 2440
|
