EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS183-01488 
Organism
Homo sapiens 
Tissue/cell
T47D-MTVL 
Coordinate
chr14:50469220-50471440 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ONECUT1MA0679.1chr14:50471085-50471099ATTATCGATTTTAA-6.3
ONECUT2MA0756.1chr14:50471085-50471099ATTATCGATTTTAA-6.27
ONECUT3MA0757.1chr14:50471085-50471099ATTATCGATTTTAA-6.03
PLAG1MA0163.1chr14:50470183-50470197GGGGCCCCCGGGGG+6.24
YY1MA0095.2chr14:50471240-50471252CAACATGGCGGC+6.37
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_01989chr14:50465559-50470968Aorta
SE_02531chr14:50465534-50470782Astrocytes
SE_10835chr14:50465467-50471273CD19_Primary
SE_12092chr14:50465522-50471323CD3
SE_12624chr14:50469154-50470066CD34_adult
SE_12624chr14:50470269-50470718CD34_adult
SE_14517chr14:50465207-50471482CD4_Memory_Primary_7pool
SE_16435chr14:50465322-50471145CD4_Naive_Primary_8pool
SE_17232chr14:50465558-50471145CD4p_CD225int_CD127p_Tmem
SE_18008chr14:50464185-50471524CD4p_CD25-_CD45ROp_Memory
SE_18398chr14:50465224-50471369CD4p_CD25-_Il17-_PMAstim_Th
SE_19249chr14:50465495-50471111CD4p_CD25-_Il17p_PMAstim_Th17
SE_20051chr14:50464037-50471405CD56
SE_20946chr14:50465190-50471276CD8_Memory_7pool
SE_21806chr14:50465556-50471115CD8_Naive_7pool
SE_23015chr14:50464221-50471304CD8_primiary
SE_23704chr14:50469056-50471322Colon_Crypt_1
SE_23843chr14:50469074-50471308Colon_Crypt_2
SE_26110chr14:50465469-50471334Duodenum_Smooth_Muscle
SE_26833chr14:50465567-50471479Esophagus
SE_27688chr14:50465422-50472685Fetal_Intestine
SE_28581chr14:50465331-50472711Fetal_Intestine_Large
SE_31801chr14:50465487-50470970Gastric
SE_33820chr14:50465576-50471385HCC1954
SE_34553chr14:50465334-50471193HCT-116
SE_34928chr14:50465509-50471474HeLa
SE_35844chr14:50465435-50471552HMEC
SE_37039chr14:50464312-50471158HSMMtube
SE_43300chr14:50469122-50471018Lung
SE_43464chr14:50468073-50471342MCF-7
SE_44190chr14:50465379-50471119NHDF-Ad
SE_44956chr14:50465535-50471037NHLF
SE_46014chr14:50465226-50470945Osteoblasts
SE_47176chr14:50463767-50471996Panc1
SE_50409chr14:50465553-50471375Sigmoid_Colon
SE_52447chr14:50465538-50471425Small_Intestine
SE_54235chr14:50465329-50471097Spleen
SE_56500chr14:50464349-50470902u87
SE_57680chr14:50469109-50470931VACO_503
SE_57995chr14:50469315-50470219VACO_9m
SE_57995chr14:50470245-50470763VACO_9m
SE_61099chr14:50426023-50471480HBL1
SE_62298chr14:50396222-50471436Tonsil
SE_64061chr14:50469100-50470451HSMM
SE_64483chr14:50465718-50471323NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr145046960050470800
Number: 1             
IDChromosomeStartEnd
GH14I049997chr145046396950476637
Enhancer Sequence
AGGAAACACC TCACTAGAGA GTGCTTGGGC ACAGGAGGTG GCATTTTGGG TTGTCACAAA 60
GATGGGGAGG TGCTACTTGC ATTTCATACA TAGGGGTTGT GGGGGCAGGG GCAGCTAGTG 120
CTGTTACAGT GATGATGCAA TGCGGCCCCG TCCCAAGTGG GGTGGGGGGC ACTGTCCTGC 180
CCTAAATGCC CACAACTCTC CCCACGCCGC TCTCCCACCC CATTGAGAAG CAGTGGTTGG 240
ACCTACGCTC AGCATTGTGC TCCCAGGCCC TCTCTGCGGG TTCAAACGCC TCTTGATGTC 300
CTCTTGGTCT CTGCCTCCTT GCTTCCTCTA GTTGGGATGC CTGCACGCTG GAGAGAGTTG 360
GGTCTTTTGT GGCTTTTGTG GCTCTGGTCC CAGTAGGAGA TGACAGACAC AACCAGAGGG 420
CAGGATTCCC TCGTTCCACG GTTCCATCTA CTCTGGAGGC GAAAAAGGGG TGTGTGAAGT 480
GGTCCCTGGG AATAAAGAGA AAGCTGCTCA CCTTTCTGAA AAACTTTTCA CCTCTCAGGG 540
AAAGGGGACC TGAGAGAAGC CTAAGAGAAA ACTCCTGATG CTTAGCCAAC TCCTTGAGAA 600
GGAAAGTGAG AATGGAGGCT GAAGCCCCTT CCATCCTTCC TGGTAAAGCA GCGGAGACGC 660
CAACACCCAC GATCTGCAAC TCAAAGTCAA GGGATTCCGT GTCCCTGCTT GTGTCAACAT 720
AGAAAACGCC CATGGCAACG GGCAAGTGCG GCCTGAAATG GCAGAGTGTG TGTTTCACAA 780
AACAGGGGTG GCTCACGGCT GCAGCCGCCC GGGGAGGTCC TGGCCTTGCC TTCGAGGGGC 840
TGGTCCTCGG GGGGTGGATG CAGCTTTGCG GGGCTGGCTC CACGTCGCGC CGCGGCGGTT 900
TGGGCTGGGG AGCAGCCCTG CAGGGAGGCG CCGCCGGGTG GGCCGCGGAG ATAGCTGCAG 960
GGCGGGGCCC CCGGGGGCGC GGGGACGCCC AGCGGCCGGA TATCAGCTGC CACGCCCGCG 1020
TGGGCGGAGA AAAGAGCAAT TTGACTTTGG ACGGAGAGCT GAGATGCGGG GAGGAAATCC 1080
ACCACCGGCC TCTGGCGACT CCTGTCCTGC GCGCAGGGGA GGCAGCGCAG CCCGTGAACA 1140
CCCCCGAGCC CGGTGCGGGC CGAGCAGTTC TCCGCACCTC CGGTAAAGGT GCAGGACCGG 1200
GTGATGGTCT CTGCAGCAGT CAGAAGGCTC CTCTCCCAGC CCAGGAACGT CTGCAATAAA 1260
TTGCTTCCAT GTGCGGGCTT CCCGCTTCCT CTTTCTCTCT CAGGGTTAAT GTGGGAAAAG 1320
GGAAGTGGCT TTTTTTTTTT TATTTTGAAA ATTAGCTTTA GGGCAAAGTC CTGCCAAGTG 1380
TGTAGTTCAA TACCCCATAT TATAGGTGAG GACACTGAGC TCCAGAGAGA TCAGATTCCA 1440
GGTCACACTG CTGGTGCGCC GCCAAACCAG GTGGAGAACG CTGGTGCCTC CGCTCCTTGG 1500
GCATTTTGAC TCCGGCATTC ATGATTGTTT TCCCTTCTTT AATACCCACT ACAGCAAAAA 1560
TTTTGTTGCT GTTTCCCTCT GTTAAGAATT ATTAAAACTT GGAGGAGGGG AAGCAAAAAG 1620
TTCTTTCAAT ATTAAATTAA AGCACTGTCT AACGAGCCCA TCTGAGAGTC ATTTGGCTAT 1680
CTAGGGGAAG GTAGCTTTGA CTTATTTTTT ACTATAAAAT AGAGTCCAAA CGTTCTTAAC 1740
TCTGAAATTA GTTAGGCCAG GAGCCCCGGC TCATGCCTGT AACCCTAGTA CTTTGGAGGC 1800
CAAGATGGAA GGATTGCTTG AGGCCAGGAG TTCAAGACTA GTGTGAGCAA CATAGCAAGA 1860
GTCCCATTAT CGATTTTAAA AAATAAAATA ACATGAGATA GTACTGTGTA GAAACTATTA 1920
AAATGTAAGT GCTGTCTGGG TACGGGAGCT CACGCCTATA ATCCCAGCAC TTTGAGAGGC 1980
TGAGGTGGGC TTGAGCTCAA GAGTTTGAGA CCAGCCTGTG CAACATGGCG GCAAAACCCC 2040
TTCTCTACAA AAAATACAAA AATTAGCTGG GCATGGTGGT GTGTGCCTGT AGTCCCAGCT 2100
ACTCTGGAGG CTGAGGTGGG AGGATGGCTT GAGCCTAGGA GGTGGAGGTT GCAGTAAACC 2160
AAGATCATGC TACTGCACGC CAGCCTGGGG GACAGAGCCA GATACTGTCT CAAAAAAAAA 2220