EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-09844 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr14:50469480-50470890 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PLAG1MA0163.1chr14:50470183-50470197GGGGCCCCCGGGGG+6.24
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
TCCCAGGCCC TCTCTGCGGG TTCAAACGCC TCTTGATGTC CTCTTGGTCT CTGCCTCCTT 60
GCTTCCTCTA GTTGGGATGC CTGCACGCTG GAGAGAGTTG GGTCTTTTGT GGCTTTTGTG 120
GCTCTGGTCC CAGTAGGAGA TGACAGACAC AACCAGAGGG CAGGATTCCC TCGTTCCACG 180
GTTCCATCTA CTCTGGAGGC GAAAAAGGGG TGTGTGAAGT GGTCCCTGGG AATAAAGAGA 240
AAGCTGCTCA CCTTTCTGAA AAACTTTTCA CCTCTCAGGG AAAGGGGACC TGAGAGAAGC 300
CTAAGAGAAA ACTCCTGATG CTTAGCCAAC TCCTTGAGAA GGAAAGTGAG AATGGAGGCT 360
GAAGCCCCTT CCATCCTTCC TGGTAAAGCA GCGGAGACGC CAACACCCAC GATCTGCAAC 420
TCAAAGTCAA GGGATTCCGT GTCCCTGCTT GTGTCAACAT AGAAAACGCC CATGGCAACG 480
GGCAAGTGCG GCCTGAAATG GCAGAGTGTG TGTTTCACAA AACAGGGGTG GCTCACGGCT 540
GCAGCCGCCC GGGGAGGTCC TGGCCTTGCC TTCGAGGGGC TGGTCCTCGG GGGGTGGATG 600
CAGCTTTGCG GGGCTGGCTC CACGTCGCGC CGCGGCGGTT TGGGCTGGGG AGCAGCCCTG 660
CAGGGAGGCG CCGCCGGGTG GGCCGCGGAG ATAGCTGCAG GGCGGGGCCC CCGGGGGCGC 720
GGGGACGCCC AGCGGCCGGA TATCAGCTGC CACGCCCGCG TGGGCGGAGA AAAGAGCAAT 780
TTGACTTTGG ACGGAGAGCT GAGATGCGGG GAGGAAATCC ACCACCGGCC TCTGGCGACT 840
CCTGTCCTGC GCGCAGGGGA GGCAGCGCAG CCCGTGAACA CCCCCGAGCC CGGTGCGGGC 900
CGAGCAGTTC TCCGCACCTC CGGTAAAGGT GCAGGACCGG GTGATGGTCT CTGCAGCAGT 960
CAGAAGGCTC CTCTCCCAGC CCAGGAACGT CTGCAATAAA TTGCTTCCAT GTGCGGGCTT 1020
CCCGCTTCCT CTTTCTCTCT CAGGGTTAAT GTGGGAAAAG GGAAGTGGCT TTTTTTTTTT 1080
TATTTTGAAA ATTAGCTTTA GGGCAAAGTC CTGCCAAGTG TGTAGTTCAA TACCCCATAT 1140
TATAGGTGAG GACACTGAGC TCCAGAGAGA TCAGATTCCA GGTCACACTG CTGGTGCGCC 1200
GCCAAACCAG GTGGAGAACG CTGGTGCCTC CGCTCCTTGG GCATTTTGAC TCCGGCATTC 1260
ATGATTGTTT TCCCTTCTTT AATACCCACT ACAGCAAAAA TTTTGTTGCT GTTTCCCTCT 1320
GTTAAGAATT ATTAAAACTT GGAGGAGGGG AAGCAAAAAG TTCTTTCAAT ATTAAATTAA 1380
AGCACTGTCT AACGAGCCCA TCTGAGAGTC 1410