Tag | Content |
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EnhancerAtlas ID | HS154-13497 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr2:239171740-239172810 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr2:239172612-239172633 | GGAAAAAGAGGGGGAGGAGGA | + | 6.08 | ZNF263 | MA0528.1 | chr2:239172618-239172639 | AGAGGGGGAGGAGGAAGAGGA | + | 6.11 | ZNF263 | MA0528.1 | chr2:239172577-239172598 | GAGGAAGGAAGAGGAGAGGAG | + | 6.13 | ZNF263 | MA0528.1 | chr2:239172571-239172592 | GAAGAAGAGGAAGGAAGAGGA | + | 6.1 | ZNF263 | MA0528.1 | chr2:239172576-239172597 | AGAGGAAGGAAGAGGAGAGGA | + | 6.23 | ZNF263 | MA0528.1 | chr2:239172640-239172661 | GGAGCAGAAAGGGGGTGGAGG | + | 6.23 | ZNF263 | MA0528.1 | chr2:239171802-239171823 | CCCACCCCCTCCCCCACCCCC | - | 6.26 | ZNF263 | MA0528.1 | chr2:239172653-239172674 | GGTGGAGGGTGAAAAGAAGGA | + | 6.54 | ZNF263 | MA0528.1 | chr2:239172615-239172636 | AAAAGAGGGGGAGGAGGAAGA | + | 6.64 | ZNF263 | MA0528.1 | chr2:239172583-239172604 | GGAAGAGGAGAGGAGTGGGGG | + | 6 | ZNF263 | MA0528.1 | chr2:239172609-239172630 | GAAGGAAAAAGAGGGGGAGGA | + | 7.21 | ZNF263 | MA0528.1 | chr2:239172668-239172689 | GAAGGAGGGGAGGAGGAGGGG | + | 7.33 | ZNF263 | MA0528.1 | chr2:239172567-239172588 | GGAGGAAGAAGAGGAAGGAAG | + | 7.5 | ZNF263 | MA0528.1 | chr2:239172624-239172645 | GGAGGAGGAAGAGGAGGGAGC | + | 8.75 | ZNF263 | MA0528.1 | chr2:239172564-239172585 | GAAGGAGGAAGAAGAGGAAGG | + | 9.24 | ZNF263 | MA0528.1 | chr2:239172621-239172642 | GGGGGAGGAGGAAGAGGAGGG | + | 9.53 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_23101 | chr2:239171015-239172295 | Colon_Crypt_1 | SE_23101 | chr2:239172391-239173998 | Colon_Crypt_1 | SE_23739 | chr2:239172492-239173253 | Colon_Crypt_2 | SE_24713 | chr2:239171194-239173278 | Colon_Crypt_3 | SE_28235 | chr2:239170362-239173208 | Fetal_Intestine | SE_29205 | chr2:239170289-239173310 | Fetal_Intestine_Large | SE_31544 | chr2:239171094-239173874 | Gastric | SE_37617 | chr2:239170986-239172881 | HSMMtube | SE_43918 | chr2:239166296-239177085 | MM1S | SE_50608 | chr2:239171348-239173468 | Sigmoid_Colon | SE_52761 | chr2:239170932-239173329 | Small_Intestine | SE_65405 | chr2:239170980-239173309 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I238261 | chr2 | 239170608 | 239173300 |
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Enhancer Sequence | AGATGAGGAG ATTGTCACTA AGAACCATCT TATTCCCTGG AAAGAGAAGA TACACTCCAA 60 ACCCCACCCC CTCCCCCACC CCCGGAGATC AAAAGTTGGA CTAACAGAAC CAGCTAGACT 120 TTTAATCAAT AGCAAACGAA GGTTCACTGT CCAGGACGCT GAAGGAGGCT CCCTCTGCTG 180 GGGCCTGAGT GCTTCAGCTC TGCGTTTCAC CTCCCAAGAG ATAAGTCATG ATCATGCTTT 240 TGTTTTCTTC CTTCCAGCAT CTTTTTCTTT TTCAGTGTCA TTCATTAGTT TGGCCACATG 300 TGACCTGGCA TGGATTTTTG CTTAACAAGT TTTGCCTGGG CCTCGGAAAA CCCTTTGTAT 360 GTGCTTCTTT TCCAGCCTGG TCTCGTGTGA CTTTGGCCTC AGCATCCAGT TGGTTTACTG 420 TGGCTTCTTT GGAGTCTCGG TGGCTGGCTG GGCCTCTGCC CTTTGAGCTC ATGCCTCCTC 480 CCAGAGCTGT GGCTTTGCTC CATTGCAGGA CGGAGCTGAA CTTCAGCAGC ACCTTCTGCT 540 TCTGTTTGTG TCCAGCGCCC TCTGCCGGCT CCACCGACCA TTTCTTCTCC CGATCTGCCT 600 CTTAACACTT GTTGCATCCA AACCAATGTT TCCTCAAACT CTGCTGCTTG TGTAGAAGGA 660 TTTTCCCTGT GAATCTTTAG ACCATGGTGC AGAACTTTCT CAAGGGCCTG GCGTTATTCT 720 TTGATTTCCT CCTTCTTGTC TGAGGCTCTC TCTTCAGGCC TCATGTTTTC CTTTGGACAG 780 GATATACAGA ATGTTCCTGG CATCCGTCCC ATCAAGGCCT TGCTGAAGGA GGAAGAAGAG 840 GAAGGAAGAG GAGAGGAGTG GGGGAACAGG AAGGAAAAAG AGGGGGAGGA GGAAGAGGAG 900 GGAGCAGAAA GGGGGTGGAG GGTGAAAAGA AGGAGGGGAG GAGGAGGGGG AGCCCTGGCT 960 GTCCTTGGGC TTTGTGAGCC AGGCCACACA CAAGGCTTCA TCAAGGAGAG CTTGCAGGCT 1020 GTGGCCCATC ATGCCAGGTG AACCTGTCTG CCAACCTCCC TGCACAGGGC 1070
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