EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS120-01861 
Organism
Homo sapiens 
Tissue/cell
LNCaP-abl 
Coordinate
chr14:50467110-50468520 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr14:50468046-50468056GGGGCGGGGC-6.02
TFAP2AMA0003.3chr14:50467919-50467930AGCCTCAGGCA+6.32
Number of super-enhancer constituents: 46             
IDCoordinateTissue/cell
SE_01989chr14:50465559-50470968Aorta
SE_02531chr14:50465534-50470782Astrocytes
SE_10835chr14:50465467-50471273CD19_Primary
SE_12092chr14:50465522-50471323CD3
SE_12624chr14:50468132-50468330CD34_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_23704chr14:50465519-50469041Colon_Crypt_1
SE_23843chr14:50466502-50469001Colon_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_39133chr14:50466521-50469020IMR90
SE_43300chr14:50465590-50469018Lung
SE_43464chr14:50465507-50468012MCF-7
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_52316chr14:50465758-50469030Skeletal_Muscle_Myoblast
SE_52447chr14:50465538-50471425Small_Intestine
SE_54235chr14:50465329-50471097Spleen
SE_56500chr14:50464349-50470902u87
SE_57680chr14:50466431-50469073VACO_503
SE_57995chr14:50466820-50468828VACO_9m
SE_61099chr14:50426023-50471480HBL1
SE_62298chr14:50396222-50471436Tonsil
SE_64061chr14:50465560-50469044HSMM
SE_64483chr14:50465718-50471323NHEK
Number: 1             
IDChromosomeStartEnd
GH14I049997chr145046396950476637
Enhancer Sequence
AAATGCCTTG GGGGACGTTG TAAACTTCAA CAGCTCTATC TGTTGTTTCA GGAATGAGGG 60
AGAAACATTC ACCAGAAGCT TCAGACTGGG AGGAGACAGA GTCTTTGAGG CAACCCAGGG 120
GCTTCTTAGC TGCAGCTGTG TCTGCTTTGA AGTTCAGTCC ACTCTCCCCA GGAAGCCAAG 180
AGGCTCTCAA GTGCTTGCAG CAGAGAAGTT TCATAGAACA GAAAGAGCAG ACAGAGGCAC 240
GCTGCGCCCT CCAGCACGGC TGCCTGGCAG GAAGCTTTGC TGAGTAACTT TGGTTTTAGT 300
TGGAAACCTT CTGTCATGTT CCTGTCGGGG CAGTGTGGGG AGTGTGGGCT GCACTGTGGC 360
GGGTGGGTTA GATTTCCTCC TTCCATGCAG TGGACAGGGA TGTGGGATGG GGGCACGAAG 420
CCATGGACAA GTGGATAACT GACCTTGAGA AGATGTAGAG GTCACCACAG AGGGTTTCCA 480
ACTCACGAAA GCATTTCTGC TATGGGAAGG ACAAGGGACG CTGGCCTATG GAACAGGCCA 540
CCGGAGATTC CAGAGCAGAG CCCTGCCCAG GCCTCCAGAC TTGTGGCTTT AATTATCCAG 600
TTAGTCATAG GTTTACTGTC ATCCAAGTTT AAGAAGCTTG ACTGTGACCC ATGTGCAAAA 660
AAAGGTTGTT CAGGCTTTTT TTTTTTTTTT AAAGCCACTC TGGGCTGTTC AGCAGGCTGA 720
GACAGGATCC CCAGAGCCCA CCAGCCCTGC AGAAGTGGGG ACTGCCTACC TGCACTTTTC 780
TTTCTTAGGC ACTTTTATCT TGAACACAGA GCCTCAGGCA TTGGCCAGTC CGGTTAGTCT 840
GGAAAAACTT GAGAGCCAAC AGTTTATTTC TGCTCTGAGG GCAGTTTCAC TAGCACAGAG 900
CACATGGCGA GCAGAGCCCA GATTACAAGG CTGGGCGGGG CGGGGCGGGG GCGGGGGCGG 960
GGGCGGGGGT GCAGGTGAGG TGCTTCGGCT CTGACGGGCG CTGGGCTGCT CACCCAGTTT 1020
TACATGGGAA GTGGTAGGGC CCTGTCTCCC CTGGCCCCTG CCCATGCCCC GGGAGAAATG 1080
GGTATGTTTG GGTGGTACCT TCCTGCATGG GCAGAGGCAG GTGATTGTAT CGCCAGCCCT 1140
GGAGCTCAGC GTGCACAGCT TGGGCTTCCA TTTGGAGGAA CCTGATCCTT GGACTTGAAC 1200
ACTCTGCTCT TTGTGTTTTG CACAACAGGA GAGTCCTGCT CCTCGCTTAG CTCAGCACAG 1260
CGAGTCCCCT GGCTTCAGCT TCCCTCCTGA GCACCTGACG GTTGTCGGTT TACTGTGACT 1320
CACTGCCATT CTATCTGCCT GGGCTTATGT TTCCAGCATC TCACCAGAGC TGTTGTGACC 1380
CATCTCCTGG GCAAAGCCTT CCACGGAGAG 1410