| Tag | Content |
|---|
EnhancerAtlas ID | HS197-20498 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr8:27218680-27220720 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA(var.2) | MA0072.1 | chr8:27219169-27219183 | TAAAATTAGGTCAT | + | 6.06 |
|
| | Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
| SE_08208 | chr8:27218876-27220303 | Brain_Inferior_Temporal_Lobe | | SE_09156 | chr8:27216720-27239058 | CD14 | | SE_10267 | chr8:27216807-27227080 | CD19_Primary | | SE_10868 | chr8:27181046-27285079 | CD20 | | SE_12034 | chr8:27217227-27222204 | CD3 | | SE_13758 | chr8:27218532-27227087 | CD34_Primary_RO01536 | | SE_14795 | chr8:27217610-27222557 | CD4_Memory_Primary_7pool | | SE_16778 | chr8:27218837-27221619 | CD4_Naive_Primary_8pool | | SE_17600 | chr8:27217455-27229236 | CD4p_CD25-_CD45RAp_Naive | | SE_18325 | chr8:27216741-27229078 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19392 | chr8:27216824-27222187 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20066 | chr8:27216778-27230915 | CD56 | | SE_21397 | chr8:27217312-27222271 | CD8_Memory_7pool | | SE_22414 | chr8:27216753-27229136 | CD8_primiary | | SE_27921 | chr8:27218674-27221105 | Fetal_Intestine | | SE_28623 | chr8:27217934-27222042 | Fetal_Intestine_Large | | SE_31168 | chr8:27218925-27226604 | Fetal_Thymus | | SE_32488 | chr8:27216612-27229104 | GM12878 | | SE_40108 | chr8:27217492-27224812 | K562 | | SE_41696 | chr8:27218982-27220305 | LNCaP | | SE_43522 | chr8:27216759-27225361 | MM1S | | SE_50221 | chr8:27218813-27227034 | Sigmoid_Colon | | SE_52630 | chr8:27218810-27227024 | Small_Intestine | | SE_53591 | chr8:27218861-27222787 | Spleen | | SE_55148 | chr8:27219032-27220487 | Thymus | | SE_59882 | chr8:27206325-27247753 | Ly4 | | SE_60867 | chr8:27217627-27263346 | DHL6 | | SE_62276 | chr8:27181124-27271753 | Tonsil | | SE_67171 | chr8:27216759-27225361 | MM1S |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr8 | 27219196 | 27220432 | | chr8 | 27219305 | 27219672 | | chr8 | 27219743 | 27220043 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I027359 | chr8 | 27216947 | 27230373 |
|
Enhancer Sequence | CCATATGTAC AAATTATTTA GCTCCAGATT TAGCTTTTTA TTTCTTTTTT GTTTCCTTTT 60
TGTTTGTTTA TTTGATATAG GGTCTTGCTC TGTTGCCCAG GCTGGAGTGC AGTGGTGCAA 120
TCATAGCTCA CTACAGCCTC GAACTCCTGG GCTCAGGTGA TCCTCCCATC TTAGCCTCCC 180
GAGTAGCTGG GACCACAGGC ATGCACCACC ATGCCTGGCT AATTTTTTAT TTTACTTTTT 240
GTACAGATGG GGGTCTCACT TTGTTGCTCC AGCTGTTCTT GAACTCCTGG CCTCAAGCGA 300
TGCTCCCACT TTAGCCTCCC AAAGTGCTGG GATTACAGGC ATGAGCCACC GCAGCCGGCC 360
TGGATTTGGC TCTTTAAAGG AAAGAGCGAG CCCTGGACTG GGCAGGGTGG GAAAATGGCC 420
CCAGCTCTCC CTCTGACTTC AGGGAGGGAC CTTGGATAGG GGGCTTATGG GCTCCAGGCA 480
CCTTCTCTGT AAAATTAGGT CATACTAAGG GAGCTGGAGG GCCCTTCTCT TTCTGGTATC 540
CCAGGTGGTC TCCCCAGGGG TGGTGGTTGT GGCTGAGGCC CACTGCCTGC TTTTCTGGTG 600
CTCTCAATGA AGTACAGTCC TGGGGTCCTC TGTATGTGGA TGGACTAGGC TGTGAAGTCT 660
ATCCGCCCCC CTGCTCCGCT CCACACCCAC ACACTGCTCT TCACTGATAA CCCCGATGAT 720
GCAGACAGCC TCCCTCAGGA ATTTTTCTCA TCCTCCTAGT CATCATTTCA GTCAGCCCTG 780
CCCCGTGTGC CAGACAAGCA CACTCTATGT GTTCAAAGGT GATGCACCGA TCGTGCCCTG 840
TCTGATGTTT ACTAACCAAC CTGACTGGGT CTGTGGGTGA CAAGGGCAGG CCCTGTTTCC 900
CTTGGATCTT CCTTTTATGG ACACAAATCG CTGACCTGTC TGGGCAGGCC TGCTCTAATC 960
CAGGTCTGGC CCTGAGCCTC CTGTCATTTT GCTGACCCAG TTCATCATCC TGGAGGCAGG 1020
GCTTGAGTTG AAAAGTTAGA GCCTCAGGGC AGCACCAGGA GCCTGCACTT TCCGGGGCCT 1080
CCCCTTCTCT CTCCCCTAGG CTGACCTGTC CTCCCCTCTC CACTTCCTGG GCGTGACTCA 1140
CAGGCAGGCC CTATCGGCAT GGCAGGTATG TGTCATTTCC TTATGCTGGT GAGACCCAGA 1200
GTTTCAGTGT TAGCACCCCC ACACTGTGGC TCTTCTAGCC CAATGGAGAA GGGCTAAGGG 1260
TTTCTAAAGT CGTTGACCTA GGGATTTACT GTTGGGATGA ATTTCTCACC TAGGGGAGGT 1320
GTTCTGTTTT TGCTGAGAGA TGACTGTGGG GAGCAGGGTT CTCTGCTCCT CTGACACTAC 1380
TCATCCTCCT TCCCAACACC TGTGGGCCTT TAGCAAAGCA ACACCCCACC CCCACCTTCA 1440
CCCTGACCCC AGCAGTGTTT TCTTTCCCCC CACCAAGACT TCCTTGGGGC CCTCTGGCCT 1500
TGCCAAACCC CCTTTGTAGC AGCCTCCCCT TCCAGCAGTG ACAGGAGGGA CCCAGCCTCG 1560
GGAGCCTGTC TCTGAGAGAC AGATGCAGGC AAAGAGCCGT TACCATGCAA AATCTAGAAC 1620
TGTTCCCACG TGAAATCTAG AACTTCTCCC ACACGAAATC TAGAACTGCT CCCACACGAA 1680
ATCTAGAACT GCTCCCATGC GAAATCTAGA ACCACTCCCA TGCGAAATCT TGAACCGCTG 1740
GGTGGAAATG AGGTTCAGTA GGTGCGGCAG TGTCACCTCT CTGGAGCATC TTCCCAAGTC 1800
TTTATGACAA ACAGGGATAC CCTCATGGCC AGAGTCAGCT GGGAATTTTT GTGGAAGCAG 1860
CTCCTTGGAT AGCATCACTC CTGTTCTCGT CATGGTGGAA AATGACTAAA AACTCAGGAT 1920
ATCCCACTGG CCCTGGGCAA ATTCCCTCAT TGGAGTAGGG ACTAGGACAA GGGCCAGCCC 1980
ATCCTGTCAG GCCAGAGCAC TTCTGTGGTC TTCAGCCCAG TTCTGAGGGC CCCTCTTGAA 2040
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