| Tag | Content |
|---|
EnhancerAtlas ID | HS098-29794 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:43155610-43158180 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr2:43156267-43156278 | CTAATCCCCTT | - | 6.32 | | GSC | MA0648.1 | chr2:43156266-43156276 | GCTAATCCCC | + | 6.02 | | RARA(var.2) | MA0730.1 | chr2:43156413-43156430 | TGTCCTCAGCATGACCT | - | 6.5 | | TBX20 | MA0689.1 | chr2:43156119-43156130 | GAGGTGTGAAG | + | 6.02 | | ZNF263 | MA0528.1 | chr2:43155678-43155699 | ACCTTCTTCCTCTCCTCCTTT | - | 6.18 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_00249 | chr2:43147958-43158400 | Adipose_Nuclei | | SE_01603 | chr2:43155354-43157948 | Aorta | | SE_12484 | chr2:43156275-43157083 | CD34_adult | | SE_13150 | chr2:43155304-43155954 | CD34_Primary_RO01480 | | SE_13150 | chr2:43156157-43157873 | CD34_Primary_RO01480 | | SE_13340 | chr2:43150657-43164489 | CD34_Primary_RO01536 | | SE_14058 | chr2:43150799-43157887 | CD34_Primary_RO01549 | | SE_26101 | chr2:43148673-43157819 | Duodenum_Smooth_Muscle | | SE_26918 | chr2:43148868-43157917 | Esophagus | | SE_29610 | chr2:43148401-43157976 | Fetal_Muscle | | SE_31955 | chr2:43148820-43158002 | Gastric | | SE_35343 | chr2:43151257-43157948 | HepG2 | | SE_37523 | chr2:43155345-43158523 | HSMMtube | | SE_41001 | chr2:43149310-43158000 | Left_Ventricle | | SE_42438 | chr2:43148679-43157913 | Lung | | SE_46306 | chr2:43155268-43159536 | Osteoblasts | | SE_46653 | chr2:43155381-43157743 | Ovary | | SE_48653 | chr2:43148624-43157941 | Right_Atrium | | SE_49917 | chr2:43149695-43157873 | RPMI-8402 | | SE_50379 | chr2:43148427-43157918 | Sigmoid_Colon | | SE_52706 | chr2:43148799-43157906 | Small_Intestine | | SE_53684 | chr2:43149056-43157985 | Spleen | | SE_54955 | chr2:43148579-43157891 | Stomach_Smooth_Muscle |
|
| | 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 |
| GH02I042921 | chr2 | 43148553 | 43161714 |
|
Enhancer Sequence | TAGGCCCTGT TGAGAGGTTT CTGGGACCGT TGGGATTTTG ATTTGACCAA TCAATGTTTT 60
ACTGTTGTAC CTTCTTCCTC TCCTCCTTTG GGTGGGAAAC CACCCAAAGG TCCCTGTCTG 120
CCTCTGATAG CTCCACTCTT CCCTCAGACC TGGCTGGGAT GGAGACCTCA AAAAGGAAGA 180
ACCGGTCAGA GTCTTGGATG CAGTCCGTAA CAACCATATA TTACATTGCT GTTTCGCACA 240
AGCCTGTGTG CTTGACATAT AAGTACTTGC TCAGTGCCAA AGGGGGCGCT CTTGGGGTGT 300
GTGGCCCAGT CCCTAAGAAG TGCAAAGTCT AAAAACTGTC CTTGGCTCCC CCAGGAGAAA 360
GCAAACTTGC ATACAGGCTG CTGTAATTCA CTTTGAGTTT TTGAGGCAAG TATAATCAGC 420
CAGTTTCCTG GTGCATGGGG CTTGATCTCA CAGATTGCAA TTTTTCCCTA AGTAGGTAGG 480
GACAGAGGTA CCTTACTCCA GAGGAGTGGG AGGTGTGAAG GCCGACAGAG ATGTTAATAC 540
CCAGTCCAGC AATCTGGGAG TCCCTGATCG CTGTCCCAGG CTGCTCTCCT CCTACATCCC 600
ACCTATAGGG GATGCTCTGG AGCCTGTGCT GCTGGAGCTT GGAGCAGCAT GGATAGGCTA 660
ATCCCCTTTA CAGGCTGTTC CTCAAATCCT CAGAATATGA CATAAAAGAA TATCCCGGGA 720
ACCAGCTCCA AAAACACTGG GGCCCAGCTG TCGCCTGAGA AGGGCCTGGT TTGCCTCTGC 780
CTGCCCCAGG TCAAGCTAGA CAGTGTCCTC AGCATGACCT GCTGCCCTCC ACTGTCCTCC 840
CGGCAGAGAT ACAGCCTCAA AAAGCCAGTA TGGACAGGTC CAGCTCTGCA GTGGACCCTG 900
CTCTCCAGAG TGGGCTGGGG AGGGAAAAGG AATGCGGTGT GTGTACACAC GTGTATACGG 960
ATGCGTGTGA GCACATGTGT GCGCTGTGTC TGGCCTGTTT GGACGGGCTT GCTTGGTACC 1020
AAGAACAGCC TCAACAGAGA TTAGAGAAAA GCCTTTGGGG CTCTCTGTAC TGCAAGCTCA 1080
CCCAGTGTCA ACAGCACCCT CTTTGGGCTC TGGACTGTGT GTAGCAAAGC CACCCCGAAA 1140
CCTCTCTCTT TCCTGGCCTT GCCTCTCGAG TCATGGCCTC TGGAGTGACA GCTCTCCTTG 1200
TGTCACTTCT CTGCCTGGTC ACCCACAATG GCTCCCAGCT TTCGGAGAAA CATTCACCAG 1260
CACACCTAAA ACACAGGGTC CCAGTGGCCC ACCTTACACT CAGGGGGCTT GATTCAGGCC 1320
CAGCCTCAAC CGGACTCTTC CTGCTAGTCC CAGACACCCT TTGTGAAGCT GTGAGAGCAG 1380
TGGATTCCCT CCCAGGAATC CTACTGATCT GTGTGCACAA GGGCCCACCC CATGAAAGGG 1440
CAAACAATTG CAGGATTCCT GGGTGCCCTG AAGCCCCTAC CCTGAGCCCA GGCTGAGAGC 1500
TTTTGTCCCA CACTTCCTAT AAGCCAGATT TGTCACTGGG CTCCCATAGG CTGCCCCTCA 1560
CCTTGTCTTC CTTCCAACAT CAGTCCAACC CCCTCCTTGT GGGGAAGACA GGAGGAAGCC 1620
TCTAGTGCCA GCTGCCTCCA CCCAATGGTG GCTCTGCCTG AATTCGGCAG GGAACCTTCA 1680
GCACAGCCCA GGGCAGCTGC TGTTGGACCC ACTCAGGGAA TTGTGTCTGA CCCGACCTAC 1740
GCATTTGGTG GTTAGCTTGC TCTGTGCAAA CAGTCCCCAG GGGACTGGAA TCCTCGCTGC 1800
AAAAATAAAT TCTCCCTCTG GACTTGCTTT TCTCATTTTG CTTTCTCTGC ATTCTGGCTT 1860
TTTCTTTTTT CTTTCTAGTG TCCCAACTGC TTTTATCTTC TTCCTTTCCT CCCACTGAGA 1920
CCCAAACAAA CCTCCTGGTA AACAAACTCT CAGGCCAGTC TCTTAAAGAG ACAGTATGTG 1980
TTTGTTGCCA TCTGGATGTC CAGTCCTGCT CAGGGGCTGC ATGAGGTCTG GGGGCAGATG 2040
GGCTGTGAGG TGTTAAAGAT CATTCAAGAG ACTCACAGGA AAAAGCTGGC CTAGAACAGT 2100
GCACCGAGAA AATTGCCCTA AGAGCCCCCT CTCCTTTCCC ACTCTCACCT GAAAATACAG 2160
AACAGGAGGG ACCAGCGGGG TTTCCCTTTA GCCAGTCTCT CTGAGTGGTG TTGTTGAGAC 2220
TATTGTCTGC TTTTGTCTGC ATGACCTGGA AAGGATTCCT TTTTTTTTTT TTTTTTTTTT 2280
TTTTTTTTTG AGACGCAGCC TTGCTCTGTC GCCCAGGCTG GAGTGCAGTG GCGCAATCTT 2340
GGCTCACTAC AACCTCCACC TCCCAGGTTC ACGCCATTCT CCTGCCTCAG CCTCCCAAGT 2400
AGCTGGGATT ACAGGTGCCC GCCACCACGC CTGGCTAATT TTTTGTATTT TTAGTAGAGA 2460
CGGGGTTTCA CCATGTTGAC CAGGCTGGTC TCGAACTCCT GACCTCAGGT GAGCCGCCCT 2520
CCTCGGCCTC CCAAAGTGCT AGGATTACAG GTGTGAGCCA CCTCGCCTGG 2570
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