| Tag | Content |
|---|
EnhancerAtlas ID | HS099-01479 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr1:159892160-159893220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr1:159892832-159892845 | AGCAGCTGTTTCT | + | 6.28 | | Tcf12 | MA0521.1 | chr1:159892831-159892842 | CAGCAGCTGTT | - | 6.32 |
|
| | Number of super-enhancer constituents: 46 | ID | Coordinate | Tissue/cell |
| SE_02009 | chr1:159887204-159896462 | Aorta | | SE_02391 | chr1:159891163-159896016 | Astrocytes | | SE_09609 | chr1:159888811-159896163 | CD14 | | SE_10233 | chr1:159889294-159896142 | CD19_Primary | | SE_10984 | chr1:159884833-159896640 | CD20 | | SE_11910 | chr1:159890466-159896330 | CD3 | | SE_12862 | chr1:159890202-159896191 | CD34_Primary_RO01480 | | SE_13325 | chr1:159887045-159896510 | CD34_Primary_RO01536 | | SE_14052 | chr1:159890274-159896187 | CD34_Primary_RO01549 | | SE_14513 | chr1:159890132-159896515 | CD4_Memory_Primary_7pool | | SE_15769 | chr1:159891344-159896220 | CD4_Memory_Primary_8pool | | SE_15949 | chr1:159891339-159896140 | CD4_Naive_Primary_7pool | | SE_16460 | chr1:159890826-159896099 | CD4_Naive_Primary_8pool | | SE_16913 | chr1:159890317-159896307 | CD4p_CD225int_CD127p_Tmem | | SE_17500 | chr1:159889525-159896840 | CD4p_CD25-_CD45RAp_Naive | | SE_17880 | chr1:159889025-159896700 | CD4p_CD25-_CD45ROp_Memory | | SE_19597 | chr1:159888663-159896506 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20057 | chr1:159890184-159896627 | CD56 | | SE_20849 | chr1:159889345-159896337 | CD8_Memory_7pool | | SE_21561 | chr1:159891197-159896204 | CD8_Naive_7pool | | SE_22506 | chr1:159889745-159896593 | CD8_primiary | | SE_23567 | chr1:159891451-159896346 | Colon_Crypt_1 | | SE_23939 | chr1:159892115-159896031 | Colon_Crypt_2 | | SE_25013 | chr1:159890918-159896336 | Colon_Crypt_3 | | SE_30108 | chr1:159891067-159896091 | Fetal_Muscle | | SE_31985 | chr1:159891083-159896707 | Gastric | | SE_34858 | chr1:159890807-159896516 | HeLa | | SE_36438 | chr1:159891272-159896570 | HMEC | | SE_38165 | chr1:159890321-159896029 | HUVEC | | SE_40207 | chr1:159890880-159896228 | K562 | | SE_41182 | chr1:159890906-159896421 | Left_Ventricle | | SE_42315 | chr1:159887173-159896572 | Lung | | SE_44957 | chr1:159891221-159895990 | NHLF | | SE_47692 | chr1:159891560-159896059 | Pancreas | | SE_48986 | chr1:159891201-159896458 | Right_Atrium | | SE_49778 | chr1:159891574-159893172 | Right_Ventricle | | SE_50509 | chr1:159888888-159896553 | Sigmoid_Colon | | SE_52604 | chr1:159889149-159896485 | Small_Intestine | | SE_53483 | chr1:159887801-159896526 | Spleen | | SE_55434 | chr1:159890662-159896015 | Thymus | | SE_58180 | chr1:159892507-159896090 | VACO_9m | | SE_59359 | chr1:159879583-159907614 | Ly3 | | SE_63031 | chr1:159879414-159896447 | Tonsil | | SE_63399 | chr1:159883649-159916570 | NCI-H69 | | SE_64771 | chr1:159890244-159896649 | NHEK | | SE_65431 | chr1:159891110-159896368 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CGAAAGCTGG GCCAGATAAA TGTCAGTCTG GGCCCCGACC CACAGCGCCA GGCACACACA 60
CCATCAGCTT GGGGAAGGCA GGCGGGGTGG GGTGGCTGAG TTCTGAGGAG AAACCAAGAG 120
AAGCATCCCT GCCCTTCCCA GAGGCCACTC CACCATAGAA ACCTCTAACC TCTGATGCAC 180
AGGGGAATGG CTGGAAGACA GGTAGGAAGA GGAAGGGGCT AAGAGCTACT ACCACCAGTA 240
AGCCCCCTTT CCGCAGCCCA GTTCCAGACC TCTCTCCTGG GAGTGGCTGT GCTCAGGGCT 300
GTTTCCAGGG ACCAAGTGGC CTGAGGCTCG GGGATCACCA TGGCACAGGT AAAGAAAGGG 360
CAGGAGAATG ATTAACCTAG ACACTGGGGT TAAGAGCAGA GAGAAAGGCC TGAAGCCAGA 420
CACTTCCAGT GCCCCCCAAC CCCCCAAGGC AGGACAAACT TGGCCTCCCA GACCCACCAC 480
TGGGTGGAAA GTGGATGCTG AGGAACCCCC TCCACCGCCC AACGCTGGGG CCTGGACACA 540
GCTGGCAGGG TCACGGCCTC CAGCTGCAGT GTATCTGCTC CACTCTGGGG CCATTGCCCT 600
CAAGCTCTGA GGTGCCAGAG CCATAGGGCG GGGTCCTGAG AAGGGGCAGT TCCAACCAGG 660
CCAGGCCTGG TCAGCAGCTG TTTCTCTTCC CCACCCCCAC GGGCAGGCAG AAGCTGATGG 720
GCTGCGGCTG CTGGAGCTGG GAAGGCCCAC CCTAGGGACA CCCAGGGGAC CTGCCCCTGC 780
CTTCCCTCAA ACATAAAGAA AACAGTAAGC AAGTTGCCTA CCAGGGTGAG AAGAGATATG 840
CCCAGCTGGA AGACAGGTGT GGGGGACCCC CAGAGCTGGG GACCCCAAAG GAAGGTGACA 900
GCTGAACAAC CTGGGGGATG GACTGGCAGG GAGCAACCTA AACCCTAGCG CTACTGCAGC 960
TGTGAGAACA ACCCTCACCC TCACCCTGGA GTTACAATAG GCGGGAAACG GGGAGGGGCC 1020
ACGCAAGGCA CTCGGCCCCA CCCAGACCCT GGGCTGGAAG 1060
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