EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS146-04502 
Organism
Homo sapiens 
Tissue/cell
NHDF 
Coordinate
chr14:50441590-50443240 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
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
Number of super-enhancer constituents: 36             
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_18008chr14:50441708-50450390CD4p_CD25-_CD45ROp_Memory
SE_18398chr14:50435547-50450215CD4p_CD25-_Il17-_PMAstim_Th
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_50518chr14:50441633-50445051Sigmoid_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: 1             
ChromosomeStartEnd
chr145044174350443087
Number: 1             
IDChromosomeStartEnd
GH14I049969chr145043578750451256
Enhancer Sequence
CCACACCCAC CTACTTTTTG TATTTTTAGT AGAGACTGGG TTTCACCATG TTGGCCAGGC 60
TGGTCTTGAA CTCCTGACCT CAGGTGATCT GCCTGCCTCA GCCTCCCAAA GTGCTGGGAT 120
TACAGGTGTG AGCCACAGCG CCTGGCCTCA CCTGGCTAAT TTTTTAAGTT TTTGGTAGAG 180
ATTGGTTCTC CCTATGTTGC CCAGGCTGTT CTTGAACTCC TGGCCTCAAG AGCTCCTGCT 240
GCTTTGGCCC CTCAAGGCAC TGGGATTATA TAAATTTACT TTTTAAATAT GTCATCTTGT 300
GCTGTATTTG TGCTTTTCCC CTTGCAAACA AATAAACAAA AAAGTTCTAG TCAATACATA 360
AATCTTTAGT GATCTGCTTA AACAAAGCTG TGGGAGCAAG AGGGTAGCAG ATTCAGAGAG 420
CAGTTTCCTA GCAAAAGTCT TTCTGCTGCT AACATCTTCC AGGTCAGCTT CCTAGGCCCC 480
AGTGACTAAG ACATTGGGAC TTTATTCTTA ACCTCCCTGG TCCAAGGCCT TTCACAGAGC 540
TAGCTGACTT CTGTGTGCTG GATATTTTTC CATGAATCAG AAATGAAATA TGCAACATTG 600
TAGCCACAAA GCAATGAAAA CAGCTCATTT GTCGTTTGTG TCCCTCCAAG CTTTGTTTTT 660
TTCTGGGTCA CACGTTATTA GTGAAGAGTC ATAATGCTAA TCCAGTTTGG ATTTATTAAC 720
AGTTGAATAG ACTATTGAGA AAAAACTTGT TAATCATCAG AAGCAAATTC ATTGCAGAAG 780
AATTACAGAC AGAGTGGGAC AAATGCCTTA AGCCAACTAA TTTTCTGCCC CTTCAGGGAA 840
AACTCTTGGA TATTGGAATT AAGTGTCACA ACTGGAAATG TAAGAATGTA ATTGCTTTTA 900
TTGAATACTT ACTATGTCCT TGATACTAAG GACAGTATTT GCCTACATTC TCTCTTAATT 960
TCATCAACTC TGTGAAGTAG GTCCTAAACC CCGTTTTATA GGTGGTGAAT GACGCAGACA 1020
TTACCAGTTG CTACCCAATG TCCATTCTTT CCTTGTTCCT TACAGAGAGG CAACCCCAAG 1080
CAGTGACTGC TTCTAGCTCA AAGTTCAGGC TCTCTGGTGA TTTCTGCGGC TGCTACTGCA 1140
GCTGTGGACA GCCATGTGAT CTGATTCTGG CCAGTGAGAC CTGAGTGGAA GTCTTCTGCA 1200
GATTTCTGGA AAAGTATTTC TTCTGGGATA TGGGCACTGC CCCTTCTTCC TTGTTCCTTC 1260
CTTCTCCCTT TCTGGAATGT GGGTGTGAGG CTTGTGGCAG AGTAGCCATG CTGTGACCTT 1320
GAGGAAGCTA TGAGGAGGAA ATCCACATTC TGAGGGTGGA GGAGCAGGAA GGTGGAAGGA 1380
ACCTGGGATA TTGCTGACAT TGTAAAGCCA CTATTCCTCC CTGGAAGGCC TACCTTCAAG 1440
ACTTGTTATG TGAAAGAAAT AAGCCATTGT TTGGTTAACC TGGTGAGGCT GGGTTTCTGT 1500
TGCAGACAAC TGAATGCAAT CCCTAAGTGA TACAGGGAAA CTGAGCTGAA AGAGTTTAAG 1560
GGACTTGCTT GCATTTCCAT ATAAAGCGAT GTCTCAAAGC TGGGTAAGAC ATGATTCCTA 1620
CGCTTAAGGT GTTTACAGCC TAGTTTGGGA 1650