| Tag | Content |
|---|
EnhancerAtlas ID | HS131-05154 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr2:54831450-54832650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr2:54832345-54832360 | AATATAAAAATAGCT | + | 6.16 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_00006 | chr2:54821772-54834554 | Adipose_Nuclei | | SE_00896 | chr2:54831531-54832397 | Adrenal_Gland | | SE_04102 | chr2:54829441-54833862 | Brain_Anterior_Caudate | | SE_07789 | chr2:54830334-54833069 | Brain_Inferior_Temporal_Lobe | | SE_11005 | chr2:54827155-54833895 | CD20 | | SE_12885 | chr2:54831248-54832051 | CD34_Primary_RO01480 | | SE_13387 | chr2:54829137-54833670 | CD34_Primary_RO01536 | | SE_14098 | chr2:54829541-54832822 | CD34_Primary_RO01549 | | SE_17333 | chr2:54821742-54834672 | CD4p_CD25-_CD45RAp_Naive | | SE_18341 | chr2:54822617-54834412 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19520 | chr2:54831532-54832562 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_25877 | chr2:54831403-54833986 | Duodenum_Smooth_Muscle | | SE_27627 | chr2:54829868-54832822 | Fetal_Intestine | | SE_28537 | chr2:54829499-54833095 | Fetal_Intestine_Large | | SE_29772 | chr2:54829351-54834138 | Fetal_Muscle | | SE_31160 | chr2:54829721-54832779 | Fetal_Thymus | | SE_31545 | chr2:54831019-54832120 | Gastric | | SE_38000 | chr2:54829339-54834345 | HUVEC | | SE_39396 | chr2:54831522-54833494 | Jurkat | | SE_40773 | chr2:54827939-54834223 | Left_Ventricle | | SE_42137 | chr2:54828042-54834229 | Lung | | SE_49296 | chr2:54830891-54832595 | Right_Atrium | | SE_50115 | chr2:54828242-54832571 | Sigmoid_Colon | | SE_52386 | chr2:54830032-54833777 | Small_Intestine | | SE_53342 | chr2:54828039-54834133 | Spleen | | SE_61167 | chr2:54784367-54847020 | HBL1 | | SE_62304 | chr2:54783676-54846716 | Tonsil | | SE_66257 | chr2:54831522-54833494 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I054595 | chr2 | 54822913 | 54834247 |
|
Enhancer Sequence | TATAAAAAAA AGAGGCCAAA TTAGCTCTCA GAAGCTTTTT TTTTCTTTCT TTCTTTCTTT 60
TCCTCTCCAT CTCTGGAGTG ACAAAACCTT TGCGGTTGTA ATTACTCCAT AGTTCTGCAA 120
ATCCTGATGC CTTGCAGAGT GTAAATGACC CAAACTCAAG GCTGGGCAGG CAGGTGGGAC 180
AGAGCCAGTG CCCCAGGAGG GATCACCCAG CCCCCTCCTT CCTCTCTAAG GGTTTTTGGT 240
CCATGCGAAG GAATTGCCCA AGGCCATACT GCTTCTTAGG CAGGGCCTGG ACTGGACTCT 300
AATAAGCAAT TAGAATTATG TTGTCAGATC CTAGAGATGT TTATGTAGCC CCTTAAGTTT 360
CCTCTCCTGT TTTAGAGCGA GAAAGAAGAT GGGCCTGGGA TGGAGATATG GCTGGTAAAG 420
GTTTAGGACT AGACGGGACC TTGGGAGGGG GAAACAGAAA AAGTGCCTGT GAAAAAAACA 480
CAGGAATCCA CGGACTGTAG TGTGAGGGGA AGGGAAGCTT CTTAAAATGA TTTAAAGGAG 540
GATCAGTAAA AATAGGCATT TCCTCAGAGG AACTGCTCTC TGCCTGCAGA GCCCCGATAG 600
TCACAGGAGT CTGGTATCGA CCCTTGGCCC CACGTTAAGG GCGTTTCAGA CTTTCCTGTC 660
AGAAGTGACA CAGAAGTGCA CATGTTGCTG TGGGGACGGA AGCATGCCGC ACTAGGGAAT 720
CCGATGGCCA ATAATGGAGG CAAGACAGAG GACGCTTCTT TCCTTTGCAG AATTAGCTGC 780
TCTTGGGGCA GGCTTCAGAA AGTGTTTACT GCTGAGAGGC GCCCCCTCCC TCTGCTCCAT 840
TGTGTTTAAT TCTCTATTGT TACCTCTTCT TCCTTTTGAG AAGATGAAGT TTGGCAATAT 900
AAAAATAGCT CTTTAAAAAA ATGAAAACCA GCCACCAGAT GGGAACCGAG TCCCTCACTT 960
CCTTTCACAT GGAAGCATGT ACCCCTCTTC CCTGTATTCT GGGTTTTTCC TGTACTGTAA 1020
AGAGGACGAG CTTTAAGTCC TGGTTCACCA CATCCTAACT AGCTGGTAGA TTGCTTCATC 1080
TCTCTGAGCC ACTGTGTCTT CATGTATAAA ATGACAGGAA TAGTAATTAT TATAATGCAG 1140
GGTTACTGTG AGGATTAGAT GTGATCACAG TTGTCAACCA CCTAGCAGGG AGAGGTGAAC 1200
|
