Tag | Content |
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EnhancerAtlas ID | HS172-00262 |
Organism | Homo sapiens |
Tissue/cell | SGBS_adipocyte |
Coordinate | chr1:37946030-37947200 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr1:37946201-37946216 | AGGTCACCTTGTCCA | + | 6.08 |
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| 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 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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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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