| Tag | Content |
|---|
EnhancerAtlas ID | HS095-00630 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:27845490-27846880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat4 | MA0518.1 | chr1:27846642-27846656 | CCTCTTCCTGGAAA | - | 6.08 |
|
| | Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
| SE_00861 | chr1:27845422-27848562 | Adrenal_Gland | | SE_03261 | chr1:27846001-27846717 | Brain_Angular_Gyrus | | SE_03939 | chr1:27845236-27851100 | Brain_Anterior_Caudate | | SE_05196 | chr1:27845131-27856743 | Brain_Cingulate_Gyrus | | SE_05814 | chr1:27844227-27851238 | Brain_Hippocampus_Middle | | SE_06945 | chr1:27845183-27851030 | Brain_Hippocampus_Middle_150 | | SE_07770 | chr1:27844238-27856992 | Brain_Inferior_Temporal_Lobe | | SE_08936 | chr1:27846345-27846549 | Brain_Mid_Frontal_Lobe | | SE_23188 | chr1:27843698-27847641 | Colon_Crypt_1 | | SE_24033 | chr1:27845579-27846944 | Colon_Crypt_2 | | SE_24711 | chr1:27843869-27847003 | Colon_Crypt_3 | | SE_26518 | chr1:27843507-27857767 | Esophagus | | SE_27625 | chr1:27843691-27857024 | Fetal_Intestine | | SE_28547 | chr1:27843416-27856986 | Fetal_Intestine_Large | | SE_29557 | chr1:27845136-27850991 | Fetal_Muscle | | SE_31031 | chr1:27846218-27856799 | Fetal_Thymus | | SE_31394 | chr1:27843780-27847429 | Gastric | | SE_33477 | chr1:27843634-27857256 | H2171 | | SE_34755 | chr1:27843588-27845742 | HeLa | | SE_35950 | chr1:27843632-27846014 | HMEC | | SE_36974 | chr1:27845141-27851091 | HSMMtube | | SE_40593 | chr1:27844098-27856916 | Left_Ventricle | | SE_42106 | chr1:27844182-27851151 | Lung | | SE_48567 | chr1:27844222-27851412 | Right_Atrium | | SE_49444 | chr1:27845663-27846615 | Right_Ventricle | | SE_50130 | chr1:27844122-27851113 | Sigmoid_Colon | | SE_52467 | chr1:27843721-27848576 | Small_Intestine | | SE_54527 | chr1:27845490-27857100 | Stomach_Smooth_Muscle | | SE_55184 | chr1:27846662-27847184 | Thymus | | SE_62007 | chr1:27846487-27856737 | Toledo | | SE_62718 | chr1:27801410-27856116 | Tonsil | | SE_63746 | chr1:27846637-27850471 | HSMM | | SE_65253 | chr1:27843908-27851025 | Pancreatic_islets | | SE_66890 | chr1:27843634-27857256 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTATACCTGG CAGGCTCCCT GGCACATAGT AGGTGCTCAA AAAATATTTG TTGAATGAAT 60
GAGTGATGAA TGAATGAATG AATTCTTTGA ATGCCATGAT AAAGAATTTG ACTCTTAGCC 120
TCCAGGAGAC GGGGATCCAT GGAAAGTTCT AAAGGAAGGC AGTGTCAGGA TGCAGCTCGT 180
ATTAGAAAGC TCACCCTGGT CGCTGTGTGG AAGATGGATT GGGGAGGGAA CGCGGGAGAC 240
TAGAGGAGGG GGAATTGAGG AGCCACTGGG GGAGACAAAG ACATAGCACT TGGGGCTGGG 300
CCTGGGAGCC CCCCTGCCTG TGAGGGCCCT GAGCCCCCTC CCAGTCCTTC CCCATCCCCC 360
TGCCAGGCCT GTTGTCTCTG AGCCCAGCGG CAGGCGGGCG GTGGGAAGAG CAGGGCTGGC 420
AAAGCTGACA CTCACTAATC ACGGCCCTCA CCCCGGAGCC GCACTAACTG TCTGGTCTCC 480
ATGGAGACAC GGCAACCTCC GGCCACTTGT TAATGGCAGC TCAACAAGGC TGCAGCGACA 540
GGGACGGGCC TGACCAGCGT GCCCAGCTCC ACACTACCTG TCCCAGCCTG GCCCTCTGCA 600
GAAGACCTCA GGGGCACCAG ACCTGGGGGA CAGGACCGGA GGTCTGGTGG CTGGACGTCT 660
CCCCAACCCC TCCGTGGCCC CGCCTCCCCT GGCACTGCCA AGCAGCGAGA GGGCAGAGGC 720
AGCCTCTGCC CAGGCTGACT CCTCTGCAGG GCTGCTGGGA AGCTGAGCTC ATGCAGGTCA 780
CCCAGGCAAG GCCAAAGGGC TGGAGGGGGA TGGTGAGGAG TGGAGCGGGG ACCTGCCCAC 840
AGCCCACACA CTAGCAGAGT GGAGGAGGGC GTGCTTTGCC TGCCCTGACA ACCCTCTGCT 900
CTGCTAGCCT GAGGCAGGGG CCCAGTTGGG AACCATCTGT CCAGAACCTC TTCCCGGTGC 960
ACTGTCACTA CATCTGAAAT GCCACCGTTA GCAACGCACT CCTTCGGGAG GCAGCATGGC 1020
ATAGCACAAA AAACACTGGT TTTGCCGTCA AGCAGGCTTG GGTGCAAGGC CTGACTCTGT 1080
TTCTCTACCT CTAAGCATTG ATTTCCCCAT CTGTAAAATG GGGGTAATCA TTGCACATAC 1140
AGGCTAACTC TTCCTCTTCC TGGAAACCTG AGCTCATTAC CTGTGATGCC TCCCCCAGAA 1200
TCTTCTTCAC CCCCACAAAC CAGCAGGGCC TCCTCCACAG TCCCCGGGCT CATCCCACAG 1260
CATGCTGCAC CTGCCTGTGA CTGTCCCACA TTTGTCCTTC CCACAGACTG AGCCCTGTGG 1320
GGTTGGGCAG AGTGAGCCTC AGGAGAGGGT GGCGAAAGAA ACAAAGGAAG GGCATGGGGG 1380
CCTCCCTCGG 1390
|
