EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-09843 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr14:50466720-50468920 
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: 45             
IDCoordinateTissue/cell
SE_01989chr14:50465559-50470968Aorta
SE_02531chr14:50465534-50470782Astrocytes
SE_10835chr14:50465467-50471273CD19_Primary
SE_12092chr14:50465522-50471323CD3
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
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr145046737550468846
Number: 1             
IDChromosomeStartEnd
GH14I049997chr145046396950476637
Enhancer Sequence
AGGGGCACAC AGAGCCACAG GCTAAACACG GTCCACAGCT TCCTGAAATC AAAGGGCTTC 60
AAAGATTTGG AAGACACATT TCTTTTGATT TTTAAAGCAA CCACACACCT ATTCTGGAAT 120
AGTGTACAAA AATCACATAG GCCATCCCGA CTCCTAACTG AATCCCCTCT TCCACCGTCA 180
GAGGACGAGG GCACTTTTTG GCATGATGGA GAGAAGCGAG GGGGCAGGGG TGGCCAGAGA 240
GACGGCTGGA GTGGAGGCGG GGGCACCAGC GTGGGGTGAA GGCAGAGGCA CCACGGGAAT 300
GTAAATTGCA GGACGCATCC TGAGGCAGTG AGTGTTCGGG GCATTCTTGT GGGTGGTCAC 360
TTGGGCCCTA GATTAAAGGC AGAAACACAG AAATGCCTTG GGGGACGTTG TAAACTTCAA 420
CAGCTCTATC TGTTGTTTCA GGAATGAGGG AGAAACATTC ACCAGAAGCT TCAGACTGGG 480
AGGAGACAGA GTCTTTGAGG CAACCCAGGG GCTTCTTAGC TGCAGCTGTG TCTGCTTTGA 540
AGTTCAGTCC ACTCTCCCCA GGAAGCCAAG AGGCTCTCAA GTGCTTGCAG CAGAGAAGTT 600
TCATAGAACA GAAAGAGCAG ACAGAGGCAC GCTGCGCCCT CCAGCACGGC TGCCTGGCAG 660
GAAGCTTTGC TGAGTAACTT TGGTTTTAGT TGGAAACCTT CTGTCATGTT CCTGTCGGGG 720
CAGTGTGGGG AGTGTGGGCT GCACTGTGGC GGGTGGGTTA GATTTCCTCC TTCCATGCAG 780
TGGACAGGGA TGTGGGATGG GGGCACGAAG CCATGGACAA GTGGATAACT GACCTTGAGA 840
AGATGTAGAG GTCACCACAG AGGGTTTCCA ACTCACGAAA GCATTTCTGC TATGGGAAGG 900
ACAAGGGACG CTGGCCTATG GAACAGGCCA CCGGAGATTC CAGAGCAGAG CCCTGCCCAG 960
GCCTCCAGAC TTGTGGCTTT AATTATCCAG TTAGTCATAG GTTTACTGTC ATCCAAGTTT 1020
AAGAAGCTTG ACTGTGACCC ATGTGCAAAA AAAGGTTGTT CAGGCTTTTT TTTTTTTTTT 1080
AAAGCCACTC TGGGCTGTTC AGCAGGCTGA GACAGGATCC CCAGAGCCCA CCAGCCCTGC 1140
AGAAGTGGGG ACTGCCTACC TGCACTTTTC TTTCTTAGGC ACTTTTATCT TGAACACAGA 1200
GCCTCAGGCA TTGGCCAGTC CGGTTAGTCT GGAAAAACTT GAGAGCCAAC AGTTTATTTC 1260
TGCTCTGAGG GCAGTTTCAC TAGCACAGAG CACATGGCGA GCAGAGCCCA GATTACAAGG 1320
CTGGGCGGGG CGGGGCGGGG GCGGGGGCGG GGGCGGGGGT GCAGGTGAGG TGCTTCGGCT 1380
CTGACGGGCG CTGGGCTGCT CACCCAGTTT TACATGGGAA GTGGTAGGGC CCTGTCTCCC 1440
CTGGCCCCTG CCCATGCCCC GGGAGAAATG GGTATGTTTG GGTGGTACCT TCCTGCATGG 1500
GCAGAGGCAG GTGATTGTAT CGCCAGCCCT GGAGCTCAGC GTGCACAGCT TGGGCTTCCA 1560
TTTGGAGGAA CCTGATCCTT GGACTTGAAC ACTCTGCTCT TTGTGTTTTG CACAACAGGA 1620
GAGTCCTGCT CCTCGCTTAG CTCAGCACAG CGAGTCCCCT GGCTTCAGCT TCCCTCCTGA 1680
GCACCTGACG GTTGTCGGTT TACTGTGACT CACTGCCATT CTATCTGCCT GGGCTTATGT 1740
TTCCAGCATC TCACCAGAGC TGTTGTGACC CATCTCCTGG GCAAAGCCTT CCACGGAGAG 1800
GCTGCCGGGC CAGCAGGAGA GGAGACCCAA TCCATCCATC AGCATTTGAA TAATTCCATC 1860
CACACATACT TCTCTTCCAA ACACCCGGGC TATTTTCCTT TCCCTGAGCC ATGCAAGCCC 1920
AAGGAGCCAG CAGGGTTGCG TGCTCTCAGG AGTAGGACAC GTCACATCAA CTTGAGTGCT 1980
CCAGGAGCCC TGCCACAATG GTTTCTTTGT GAGATCATCT TTGCAGCGGT TTCCTGAAGC 2040
TCTGGCCTCC TTCCTGGTAT CTTCACACAT TCTAGGTGTT TCAATTCAGT AAAAACATAA 2100
GGGCCTTTTG ACTGCTCACT CCTGCACTTC ACACTGGGAA GGACACAGAA GTCCCCAGAG 2160
AGTGCCCTGG ACGACAAAAT GTAGTTCAGA GGTATCTAAG 2200