| Tag | Content |
|---|
EnhancerAtlas ID | HS156-00363 |
Organism | Homo sapiens |
Tissue/cell | P493-6 |
Coordinate | chr1:37946030-37947200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr1:37946201-37946216 | AGGTCACCTTGTCCA | + | 6.08 |
|
| | Number of super-enhancer constituents: 48 | ID | Coordinate | Tissue/cell |
| SE_00995 | chr1:37938982-37953203 | Adrenal_Gland | | SE_01903 | chr1:37938631-37947265 | Aorta | | SE_02806 | chr1:37939303-37946304 | Astrocytes | | SE_03113 | chr1:37939485-37946213 | Bladder | | SE_11493 | chr1:37938939-37953541 | CD20 | | SE_12046 | chr1:37940254-37947844 | CD3 | | SE_14941 | chr1:37937245-37947509 | CD4_Memory_Primary_7pool | | SE_15766 | chr1:37939160-37946281 | CD4_Memory_Primary_8pool | | SE_16682 | chr1:37938107-37946314 | CD4_Naive_Primary_8pool | | SE_16974 | chr1:37938355-37946601 | CD4p_CD225int_CD127p_Tmem | | SE_17494 | chr1:37937374-37948402 | CD4p_CD25-_CD45RAp_Naive | | SE_17864 | chr1:37936810-37948825 | CD4p_CD25-_CD45ROp_Memory | | SE_18659 | chr1:37937079-37948798 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19263 | chr1:37938768-37948200 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20187 | chr1:37940169-37947969 | CD56 | | SE_21053 | chr1:37938277-37946889 | CD8_Memory_7pool | | SE_21794 | chr1:37937265-37946727 | CD8_Naive_7pool | | SE_22516 | chr1:37940241-37948736 | CD8_primiary | | SE_23342 | chr1:37938990-37947224 | Colon_Crypt_1 | | SE_23956 | chr1:37943159-37946902 | Colon_Crypt_2 | | SE_23956 | chr1:37946960-37947657 | Colon_Crypt_2 | | SE_26141 | chr1:37940163-37946771 | Duodenum_Smooth_Muscle | | SE_26814 | chr1:37938717-37948080 | Esophagus | | SE_27863 | chr1:37940170-37946643 | Fetal_Intestine | | SE_28852 | chr1:37938631-37946719 | Fetal_Intestine_Large | | SE_31547 | chr1:37938860-37953351 | Gastric | | SE_34808 | chr1:37936154-37948891 | HeLa | | SE_36403 | chr1:37938817-37947080 | HMEC | | SE_37759 | chr1:37936023-37946583 | HSMMtube | | SE_41638 | chr1:37939130-37946581 | LNCaP | | SE_41638 | chr1:37946604-37947960 | LNCaP | | SE_42562 | chr1:37938719-37953498 | Lung | | SE_45338 | chr1:37939465-37946295 | NHLF | | SE_46585 | chr1:37936537-37947165 | Osteoblasts | | SE_47620 | chr1:37940083-37946187 | Pancreas | | SE_47620 | chr1:37946720-37947227 | Pancreas | | SE_48484 | chr1:37938688-37947276 | Psoas_Muscle | | SE_49357 | chr1:37938923-37946330 | Right_Atrium | | SE_50165 | chr1:37938796-37948704 | Sigmoid_Colon | | SE_52446 | chr1:37938826-37947998 | Small_Intestine | | SE_54020 | chr1:37938881-37946627 | Spleen | | SE_56449 | chr1:37936737-37946690 | u87 | | SE_57614 | chr1:37944458-37946554 | VACO_503 | | SE_58251 | chr1:37944087-37946233 | VACO_9m | | SE_62625 | chr1:37936685-37953308 | Tonsil | | SE_64577 | chr1:37940283-37947002 | NHEK | | SE_65323 | chr1:37939205-37953672 | Pancreatic_islets | | SE_67957 | chr1:37936737-37946690 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGAGTGGTG CCTCTGGAGG TGGGATGGTC TTACTGCCCC AGCAGCCCTG GTTCTCCCCA 60
AGAGAGACCC TCTGGGAGTG ACCTACAACT TCTAGAACTC AAGCAGGGAC CAGCATTTCT 120
TTTCTCAGTT TTTTCTGTCC TTAGCAACCT GCTCTGAATG GTGGTCATTG GAGGTCACCT 180
TGTCCAGTCT TCTGCCTCAG ATCTGGAGCC CCTCCCTCAT CCTACTGGTG GGCAGGTCGC 240
TCTTTCAACA TCCCCAGTGG CAGAAGCGCA GTATCACATA GTGGTTAAGC CTGTGGGCTC 300
TGAGTCGAGA CAGCCAGAGT TGGAATCCTG GCTCTGTCCC CTCTTGGCGC CCTGGCCTGG 360
ACAGGGACCC CTCTTAGCCC TGCTCTGAGC CACATGCTCC TCATCTGAAA CATGGGGTCG 420
GTGTCAGCAG GGGGTGTTGA CAGCATTGCC TTCCTCGTGA GGTCATATAA GTTAACACAC 480
GGTAAGTGCT GAGAAGAGTA CCTGGCACAT GGTAGATGCT CAGTGTATGT TAGCTGTTAC 540
CACTGTTCTT GCAAGAGCCC CCAGCCTTTG GAGGTAAAAA CTGAATCAGT TTCTCTAGAA 600
GTCTTGAGAT CTGGGGGCAG CCTGTCTGGG ACTGTAGGCT CCAGGAAGAG GGGCCCTTTC 660
CACTTGCACA CTTCTGTGTC CCTGTGGTCC CAGCAGCTCC CCAGGTGGGG CATGGTGAGT 720
GGCCTGACCT TTTCCCACCA TGGGATTTAG CGACCTTGTC CTGGCAATGC AAGGGACAGA 780
GCCAAGATAC TTCTCCCACC CCAGAGCAAG CTGCGGCTCA TTCACGGACC CCTCAGAACA 840
GGCTGGATGA AAGCCAAAGC CAAGACCACA TCTGGCTTGA ACAGGCCTGA TGTCCAGAAG 900
GAGAAAAGGA ACAAGGCCAG CTCTGTGCTT GGAGCCTCTG CCATGCAGGC CCTGCCGCCT 960
GTGTTCAGAT GTTCTTGGTC TTCAGGCAGC AAACTGTGCC ACGCCAAGGG AGGGGCTGGG 1020
GCATGGAAGA GGCCTCAGCA GAGTTAGTTC TTGCCCCGGT GACCTTGGCG TTAACCACTC 1080
CTGTGTGTGG CCATCAGCAG GTTAGGGAGC CCTGTAGGCC TGGCTCTAGG TCCCGCTGGG 1140
CCCTGACCTG TGTGCACCCG TCACCTCCCA 1170
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