EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-23960 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr14:50441060-50443250 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr14:50441276-50441297GTTTACTTTTTCTTTTCTTTT+6.37
Nr2f6(var.2)MA0728.1chr14:50441656-50441671TGAACTCCTGACCTC-6.22
ZNF263MA0528.1chr14:50442950-50442971GGAGCAGGAAGGTGGAAGGAA+6.01
ZNF263MA0528.1chr14:50442941-50442962GAGGGTGGAGGAGCAGGAAGG+6.19
ZNF263MA0528.1chr14:50442947-50442968GGAGGAGCAGGAAGGTGGAAG+6.49
ZfxMA0146.2chr14:50441061-50441075CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_01989chr14:50441624-50442231Aorta
SE_01989chr14:50442447-50443366Aorta
SE_02531chr14:50441707-50443216Astrocytes
SE_10422chr14:50442499-50448200CD19_Primary
SE_11322chr14:50434928-50450149CD20
SE_12397chr14:50442293-50443217CD3
SE_14517chr14:50441528-50443207CD4_Memory_Primary_7pool
SE_18008chr14:50436287-50441310CD4p_CD25-_CD45ROp_Memory
SE_18008chr14:50441708-50450390CD4p_CD25-_CD45ROp_Memory
SE_18398chr14:50435547-50450215CD4p_CD25-_Il17-_PMAstim_Th
SE_19249chr14:50436647-50441600CD4p_CD25-_Il17p_PMAstim_Th17
SE_19249chr14:50441667-50450951CD4p_CD25-_Il17p_PMAstim_Th17
SE_23843chr14:50441942-50442271Colon_Crypt_2
SE_23843chr14:50442477-50443521Colon_Crypt_2
SE_26110chr14:50441478-50444824Duodenum_Smooth_Muscle
SE_26864chr14:50441633-50444813Esophagus
SE_27688chr14:50441593-50444689Fetal_Intestine
SE_28581chr14:50441394-50444846Fetal_Intestine_Large
SE_31801chr14:50442437-50443241Gastric
SE_33888chr14:50441630-50443360HCC1954
SE_34928chr14:50441414-50443665HeLa
SE_37039chr14:50436659-50444504HSMMtube
SE_39133chr14:50441633-50443239IMR90
SE_43300chr14:50442533-50443197Lung
SE_44190chr14:50441571-50443437NHDF-Ad
SE_44956chr14:50440992-50443338NHLF
SE_46014chr14:50440951-50443576Osteoblasts
SE_47176chr14:50432303-50449980Panc1
SE_50518chr14:50436606-50441475Sigmoid_Colon
SE_50518chr14:50441633-50445051Sigmoid_Colon
SE_52316chr14:50441400-50443482Skeletal_Muscle_Myoblast
SE_52447chr14:50441664-50444873Small_Intestine
SE_56500chr14:50441594-50443749u87
SE_58661chr14:50425951-50447448Ly1
SE_60380chr14:50426505-50445615Ly4
SE_60743chr14:50425923-50445269DHL6
SE_61099chr14:50426023-50471480HBL1
SE_62298chr14:50396222-50471436Tonsil
SE_64061chr14:50441400-50443543HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr145044133550441495
chr145044174350443087
Number: 1             
IDChromosomeStartEnd
GH14I049969chr145043578750451256
Enhancer Sequence
GCCCGCCTCG GCCTCCAAAG AAAAAAGGAT TCCTCTTTCT GCTGGGGTTC CTAAGCTGGT 60
GGGTTCCTGT TTGGGAGCTT TAAGGGGCCA CTTTTGTTAC CATGGAGGGA GAAACTGAGA 120
CATGAAAGGA AGATTCCTGA ATCCTTCGTT TGAGCACCTG GAGCCAGTTA TGCCTGAAAC 180
TCTATGCCTG GACATTTTAG TCACTCAAAC CAATAAGTTT ACTTTTTCTT TTCTTTTCTT 240
TTCTTTTCTT TTTTTTTTTT TTTTAAAGAG ATAGTATCTT ACTGTGTTGC CCAGGCTGGA 300
ATGCAGTGGT GCAATCATAG CCCACTGTAA CCTTGAACTT CTGGGCTCAA GCAATCCTCT 360
CGCCTGGCTA ATTTTTTTTC CTTTTTCTTT TTTTCGAGAT GGTGTCTCCC TCTGTCACCC 420
AGGCTGGAGC GCAGTGGAGC GATCTTGGTT CACTGCAATC TCCGCCTCCC TGGTTCAAGC 480
GATTCTCCTG CCTCAGCCTC CTGAGTAGCT GGGATTACAG GTGTGCGCCA CCACACCCAC 540
CTACTTTTTG TATTTTTAGT AGAGACTGGG TTTCACCATG TTGGCCAGGC TGGTCTTGAA 600
CTCCTGACCT CAGGTGATCT GCCTGCCTCA GCCTCCCAAA GTGCTGGGAT TACAGGTGTG 660
AGCCACAGCG CCTGGCCTCA CCTGGCTAAT TTTTTAAGTT TTTGGTAGAG ATTGGTTCTC 720
CCTATGTTGC CCAGGCTGTT CTTGAACTCC TGGCCTCAAG AGCTCCTGCT GCTTTGGCCC 780
CTCAAGGCAC TGGGATTATA TAAATTTACT TTTTAAATAT GTCATCTTGT GCTGTATTTG 840
TGCTTTTCCC CTTGCAAACA AATAAACAAA AAAGTTCTAG TCAATACATA AATCTTTAGT 900
GATCTGCTTA AACAAAGCTG TGGGAGCAAG AGGGTAGCAG ATTCAGAGAG CAGTTTCCTA 960
GCAAAAGTCT TTCTGCTGCT AACATCTTCC AGGTCAGCTT CCTAGGCCCC AGTGACTAAG 1020
ACATTGGGAC TTTATTCTTA ACCTCCCTGG TCCAAGGCCT TTCACAGAGC TAGCTGACTT 1080
CTGTGTGCTG GATATTTTTC CATGAATCAG AAATGAAATA TGCAACATTG TAGCCACAAA 1140
GCAATGAAAA CAGCTCATTT GTCGTTTGTG TCCCTCCAAG CTTTGTTTTT TTCTGGGTCA 1200
CACGTTATTA GTGAAGAGTC ATAATGCTAA TCCAGTTTGG ATTTATTAAC AGTTGAATAG 1260
ACTATTGAGA AAAAACTTGT TAATCATCAG AAGCAAATTC ATTGCAGAAG AATTACAGAC 1320
AGAGTGGGAC AAATGCCTTA AGCCAACTAA TTTTCTGCCC CTTCAGGGAA AACTCTTGGA 1380
TATTGGAATT AAGTGTCACA ACTGGAAATG TAAGAATGTA ATTGCTTTTA TTGAATACTT 1440
ACTATGTCCT TGATACTAAG GACAGTATTT GCCTACATTC TCTCTTAATT TCATCAACTC 1500
TGTGAAGTAG GTCCTAAACC CCGTTTTATA GGTGGTGAAT GACGCAGACA TTACCAGTTG 1560
CTACCCAATG TCCATTCTTT CCTTGTTCCT TACAGAGAGG CAACCCCAAG CAGTGACTGC 1620
TTCTAGCTCA AAGTTCAGGC TCTCTGGTGA TTTCTGCGGC TGCTACTGCA GCTGTGGACA 1680
GCCATGTGAT CTGATTCTGG CCAGTGAGAC CTGAGTGGAA GTCTTCTGCA GATTTCTGGA 1740
AAAGTATTTC TTCTGGGATA TGGGCACTGC CCCTTCTTCC TTGTTCCTTC CTTCTCCCTT 1800
TCTGGAATGT GGGTGTGAGG CTTGTGGCAG AGTAGCCATG CTGTGACCTT GAGGAAGCTA 1860
TGAGGAGGAA ATCCACATTC TGAGGGTGGA GGAGCAGGAA GGTGGAAGGA ACCTGGGATA 1920
TTGCTGACAT TGTAAAGCCA CTATTCCTCC CTGGAAGGCC TACCTTCAAG ACTTGTTATG 1980
TGAAAGAAAT AAGCCATTGT TTGGTTAACC TGGTGAGGCT GGGTTTCTGT TGCAGACAAC 2040
TGAATGCAAT CCCTAAGTGA TACAGGGAAA CTGAGCTGAA AGAGTTTAAG GGACTTGCTT 2100
GCATTTCCAT ATAAAGCGAT GTCTCAAAGC TGGGTAAGAC ATGATTCCTA CGCTTAAGGT 2160
GTTTACAGCC TAGTTTGGGA GTCCACTGCA 2190