Tag | Content |
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EnhancerAtlas ID | HS059-24650 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr2:28589380-28590120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr2:28589551-28589572 | GCTGCTGACCAGGGTGCTGTG | - | 6.47 |
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| Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
SE_02920 | chr2:28588830-28589720 | Bladder | SE_02920 | chr2:28589759-28590234 | Bladder | SE_20015 | chr2:28587967-28590538 | CD56 | SE_22508 | chr2:28588469-28590455 | CD8_primiary | SE_23078 | chr2:28588713-28591152 | Colon_Crypt_1 | SE_23736 | chr2:28588779-28590450 | Colon_Crypt_2 | SE_24706 | chr2:28588677-28590427 | Colon_Crypt_3 | SE_25842 | chr2:28588940-28590574 | Duodenum_Smooth_Muscle | SE_27724 | chr2:28587769-28590497 | Fetal_Intestine | SE_28654 | chr2:28587645-28591460 | Fetal_Intestine_Large | SE_31386 | chr2:28587824-28591307 | Gastric | SE_34659 | chr2:28587812-28590840 | HeLa | SE_50076 | chr2:28587915-28591223 | Sigmoid_Colon | SE_52349 | chr2:28587909-28591455 | Small_Intestine | SE_53354 | chr2:28588976-28590205 | Spleen | SE_62927 | chr2:28581266-28660518 | Tonsil |
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| 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 |
GH02I028364 | chr2 | 28587674 | 28591087 |
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Enhancer Sequence | CTTTGGGGGT GTTGCCCTGG TGGAGGCTAG GGGTGGGATC AGAACCTAAT GGAAACACCA 60 CAGGGGGCAG GAGGGGATGT GGCCAGGTCG GGTGTGACCA GGATTGGTTG TGCGGCCTTG 120 TCCAGGGCTG GCACTGATAA GATCCAAGGC GGTGTCCGCT GAATGAACCA GGCTGCTGAC 180 CAGGGTGCTG TGAGCAATTC CCATCGCTTC CCTCTGGGCT GTGAGGCTCC TGCGCTGTAA 240 TATTTCTCTT CCTTTCTTAA TGCTGATTTC GTTGTGTGTA GGGTAGAGTT CAGAGGCTGG 300 CTAAGCCTTT AAAGGCTCCT TTTTTGAGTC TTGGCCAGGC CAACCCATGG CCCAGCCCCT 360 ATCTCAAAGC CAGGCACTCC CTCTTATCAG ATAAGAAACC ACGACTCAGA GAGAGGAAGC 420 TAGCTGTTCA AAGTCACAGT CGGTGGTTGG GCCAGGAAAC GGGACCCACT TCTCCCTCCC 480 AGGCCTTCCT CATGTGCAAT GCAGGCCCCC AGCTCAGGCC ACGCTCCTCT GCCTAGCGAG 540 GGTCCCAGCC TCTCTGCCTG CATCTGGCTT CACGCACACT TTCCGAGGGC AGGGGCTGCC 600 CGGCTGCTAC AAGCCGCAGT GGTAGGGCAG TGACTTGGCT GAGGGGGACA TGGGGCTTGT 660 CATTCCTCCC AGGGCTTCTC CAGGAAGTGA CAGCCAGAAG GGCCCTGGGA GGCCGCTTGG 720 TTCGATCCCA CCCCCCTTTC 740
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