EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-17196 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr14:50469130-50470790 
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
Number: 1             
IDChromosomeStartEnd
GH14I049997chr145046396950476637
Enhancer Sequence
TTCATATAAC ACCTACTTAT ATATGAAGGA ACTAATTGAG GTCTTTTGAG ATATATTTTA 60
GGAAATGATC TAACAGTGGT TTTTAACCTA AGGAAACACC TCACTAGAGA GTGCTTGGGC 120
ACAGGAGGTG GCATTTTGGG TTGTCACAAA GATGGGGAGG TGCTACTTGC ATTTCATACA 180
TAGGGGTTGT GGGGGCAGGG GCAGCTAGTG CTGTTACAGT GATGATGCAA TGCGGCCCCG 240
TCCCAAGTGG GGTGGGGGGC ACTGTCCTGC CCTAAATGCC CACAACTCTC CCCACGCCGC 300
TCTCCCACCC CATTGAGAAG CAGTGGTTGG ACCTACGCTC AGCATTGTGC TCCCAGGCCC 360
TCTCTGCGGG TTCAAACGCC TCTTGATGTC CTCTTGGTCT CTGCCTCCTT GCTTCCTCTA 420
GTTGGGATGC CTGCACGCTG GAGAGAGTTG GGTCTTTTGT GGCTTTTGTG GCTCTGGTCC 480
CAGTAGGAGA TGACAGACAC AACCAGAGGG CAGGATTCCC TCGTTCCACG GTTCCATCTA 540
CTCTGGAGGC GAAAAAGGGG TGTGTGAAGT GGTCCCTGGG AATAAAGAGA AAGCTGCTCA 600
CCTTTCTGAA AAACTTTTCA CCTCTCAGGG AAAGGGGACC TGAGAGAAGC CTAAGAGAAA 660
ACTCCTGATG CTTAGCCAAC TCCTTGAGAA GGAAAGTGAG AATGGAGGCT GAAGCCCCTT 720
CCATCCTTCC TGGTAAAGCA GCGGAGACGC CAACACCCAC GATCTGCAAC TCAAAGTCAA 780
GGGATTCCGT GTCCCTGCTT GTGTCAACAT AGAAAACGCC CATGGCAACG GGCAAGTGCG 840
GCCTGAAATG GCAGAGTGTG TGTTTCACAA AACAGGGGTG GCTCACGGCT GCAGCCGCCC 900
GGGGAGGTCC TGGCCTTGCC TTCGAGGGGC TGGTCCTCGG GGGGTGGATG CAGCTTTGCG 960
GGGCTGGCTC CACGTCGCGC CGCGGCGGTT TGGGCTGGGG AGCAGCCCTG CAGGGAGGCG 1020
CCGCCGGGTG GGCCGCGGAG ATAGCTGCAG GGCGGGGCCC CCGGGGGCGC GGGGACGCCC 1080
AGCGGCCGGA TATCAGCTGC CACGCCCGCG TGGGCGGAGA AAAGAGCAAT TTGACTTTGG 1140
ACGGAGAGCT GAGATGCGGG GAGGAAATCC ACCACCGGCC TCTGGCGACT CCTGTCCTGC 1200
GCGCAGGGGA GGCAGCGCAG CCCGTGAACA CCCCCGAGCC CGGTGCGGGC CGAGCAGTTC 1260
TCCGCACCTC CGGTAAAGGT GCAGGACCGG GTGATGGTCT CTGCAGCAGT CAGAAGGCTC 1320
CTCTCCCAGC CCAGGAACGT CTGCAATAAA TTGCTTCCAT GTGCGGGCTT CCCGCTTCCT 1380
CTTTCTCTCT CAGGGTTAAT GTGGGAAAAG GGAAGTGGCT TTTTTTTTTT TATTTTGAAA 1440
ATTAGCTTTA GGGCAAAGTC CTGCCAAGTG TGTAGTTCAA TACCCCATAT TATAGGTGAG 1500
GACACTGAGC TCCAGAGAGA TCAGATTCCA GGTCACACTG CTGGTGCGCC GCCAAACCAG 1560
GTGGAGAACG CTGGTGCCTC CGCTCCTTGG GCATTTTGAC TCCGGCATTC ATGATTGTTT 1620
TCCCTTCTTT AATACCCACT ACAGCAAAAA TTTTGTTGCT 1660