EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-13139 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr14:50333650-50336150 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZfxMA0146.2chr14:50333932-50333946CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00765chr14:50333992-50336201Adipose_Nuclei
SE_09576chr14:50334033-50337802CD14
SE_10599chr14:50334104-50337580CD19_Primary
SE_11096chr14:50333539-50339390CD20
SE_12440chr14:50334282-50335987CD3
SE_13687chr14:50334042-50335876CD34_Primary_RO01536
SE_14679chr14:50334123-50336212CD4_Memory_Primary_7pool
SE_15756chr14:50333996-50336021CD4_Memory_Primary_8pool
SE_16123chr14:50334427-50335886CD4_Naive_Primary_7pool
SE_16695chr14:50334068-50336069CD4_Naive_Primary_8pool
SE_18438chr14:50333984-50336198CD4p_CD25-_Il17-_PMAstim_Th
SE_19324chr14:50334089-50335907CD4p_CD25-_Il17p_PMAstim_Th17
SE_20104chr14:50334006-50337438CD56
SE_21237chr14:50334033-50336208CD8_Memory_7pool
SE_21722chr14:50334033-50336067CD8_Naive_7pool
SE_22278chr14:50333968-50336018CD8_Naive_8pool
SE_22837chr14:50333983-50336850CD8_primiary
SE_23303chr14:50334241-50334973Colon_Crypt_1
SE_23303chr14:50335002-50335628Colon_Crypt_1
SE_23303chr14:50335787-50336170Colon_Crypt_1
SE_24603chr14:50334338-50334959Colon_Crypt_2
SE_24603chr14:50335010-50335534Colon_Crypt_2
SE_25036chr14:50334350-50336082Colon_Crypt_3
SE_26328chr14:50334059-50336156Duodenum_Smooth_Muscle
SE_26732chr14:50333843-50335723Esophagus
SE_26732chr14:50335793-50336365Esophagus
SE_27777chr14:50334068-50336154Fetal_Intestine
SE_28725chr14:50333995-50336010Fetal_Intestine_Large
SE_29997chr14:50334173-50335973Fetal_Muscle
SE_34956chr14:50334024-50336109HeLa
SE_52966chr14:50334193-50335805Small_Intestine
SE_54002chr14:50334175-50335700Spleen
SE_55560chr14:50334310-50335555Thymus
SE_59312chr14:50327340-50367097Ly3
SE_60830chr14:50327790-50364534DHL6
SE_61265chr14:50327065-50374962HBL1
SE_62348chr14:50327484-50374966Tonsil
SE_64446chr14:50334201-50336000NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr145033484650335244
Number: 1             
IDChromosomeStartEnd
GH14I049867chr145033404550337750
Enhancer Sequence
ATGCACAACC TCGAATCAGC CGTTTGCTTT TTTTTTTTTT TTTTTTTTTT TTGAGACGGA 60
GTCTCGCTCT GTCGCCAAAG CTGTAGTGCA GTGACGCGAT CCCAGCTCAC TGCAAGCTTC 120
GGCTCCCGGG TTCACGCCAT TCTCCTGCCT CAGCCTCTCG AGTAGCTAGC TGGGACTACA 180
GGAGCCCGCC ACCACGCCCA GCTTTTTTGT TTGTTTTTTC AGTAGAGACG GGGTTTCACC 240
GTGTTAGCCA GGATGGTCTC GATCTCCTGA CCTCGTGTTC CGCCCGCCTC GGCCTCCCAA 300
AGTGCTGGGA TTACAGGCGT GAGCCACCGC GCCCGGCCAG CCGTTTGCTT TTTTAACAGT 360
GCAAAAAACA AGGCCGTGTC TGGCTATATG GGGCTTTGCT TGTTCAAAAT GTAACCTCTA 420
TACGGCCGCG CGCAGTGGCT CACGCCTGTA ATCCTAGCAC TTTGTAAGGC CCCGGCAGGC 480
GGATCACTTG AGGGCAGGAG TTCGAGGCCA GCCTGGCCAA CATGGTGAAA CCCCATCTCT 540
ACTAAAAATA CAAAAATTAG CCTGGCCTGG TGGCGCGCGC CTGTAGTCCC AGTTATTCAG 600
GAGGCTAAGG CAGGAGAATC GCTTGAACCC GGGAAGAGGA GGTTGCAGTA AGCCGAGACG 660
TGCAACTGCA TTCCAGTCTG GGCAAGACTC CGTCTCAAAA AAAAAAAAAA AAAAAGTAAC 720
CTGTATGAAA GTTAATTTTG TGGCACTGAA CATTGGAGTA GATAATAACC TCATCTGAAA 780
TGGGATGTCT CAATCTGTCT ACAAAAAACT CCATGCCATA GAGCTCAAAA GTTTGTAAAT 840
TAGTCCTTTG GAGACGTTAA AGAGCATGGA GTCATACGAA AAGGCTTTCT GCCCTGGTAA 900
GGGAAGAAAG CTTGTGGGCA GGTTGAGTCT GGTCCTTGAG TTCTCAGCTC TCACCAGGGA 960
AGGGGTACCA GACAAAGCTG AGGCTGAACT TGAGCCGCAC AGGCCCTGAT TGCTGGGCCG 1020
TGAGAGAACA CCCGAGGAGG GGGCCCAACG CACCTGAAGA AAAGACGACG TGGAGGTCAT 1080
AAACGACCAA GAGAAAGGGG CGCACCGCGG ACACTATCGC CAGCCGGACC CCAGATCAAG 1140
AGAAATAGAA GAGGAGCCGG GGTCTCCAAA CACTACAGGC TGGGGTCCCA GGGCAAGGGA 1200
CTGGGCCGCC GGCGGAAGCG TCGGGGAGAG GCGGGACTGT CGGCGGGGTG TGGGAGAGGC 1260
GGGGCGTGGG AGAGGCGGGG CGTGGGAGAG GCGGGGCCAC CAGCAAGTGG GCGGGCGGGA 1320
GGCGGGGCCG CAGTTGGGGT GTGGAAGAGG TGGGGCAGCC AGCAACTGGG AGGGGAGGGA 1380
GGCGGGGCCG CCGGCGGGGC GCGGTGAAGA GGCAGGCTGC CAGAGTGCCT GGCCGACAAA 1440
TTACCCAGCG TGAGCTCGGT CACCTGGGTG TGGCGGTTCA ACCCTGAGCT ACGTCCTCCC 1500
ACGGCGCCCG GAGTTTCCCC ACCCTTGACA CAATGCCTAT TCGCAGCTCG CTGCAGCGGA 1560
GTCATCTACT GCTGCTGGCA GGATTTTCAT TGCGACGGGT TGTTATGTGC ATTTCAGGAC 1620
ATACCCCGTG GGTTGTCCCT GATTCAGTTA CATTTAATAA ACGAGCGGTG GATTAACCGG 1680
AATTACAGTT TGACAGAAAA CACGTTTTCT TCTCGACAAC ACCCTGCGTG TAGGAAGAGC 1740
CTTTAATATG GTTGATACAC AATATTTAAT CGATCCAGAA ACACATTTCT TGTGACAGGC 1800
TTTTAAATAT CAGAATAAAT CCTAAGAGTG AACAGTTGAA GTTACTTATC CAATGTTACA 1860
CTGCTAGGCC TATAAATAAA CTTGCGGGGT CTATTTTCTC CCATTTGAAT ATGCTTTGAT 1920
TTCCATATGA CAGTTCTGCC GAAATGTTTT GACATTTTAG ATCTTAGTAG AACTCCATTA 1980
CAACACGACT ATTTATTACG TTGATTCTGA TCTGACGTGT AATAAATCAT GTCCCCAAAC 2040
CAAAACTCCA TACATTAATA TCCTGATATT TAACACACTT TATCCAACTA TTGATTCTAT 2100
CTGTTCACAC CAATGTGGTA AAAGCTTTAT GTTGTATTTA ATTTATTCAT TTTGAAAATA 2160
TTTAAAATGC TTCATTTTCA TTAGCTAACT TTGAAGAGTG CTTCTTTTGT TTGGGGACTC 2220
TGTAGATTTA GGCTAATGTC ACCATTCAGA ATAATTGGCA AATTGATTTG CCTTTCTTTG 2280
ACTTTCTATT CTCCAAGCTG ATTATACGCT GAGGTTAACA CATTTGAACT GGCCGGCCGG 2340
TTGGGTGGCT CACGCTTGTA ATGCCAGCAC TTTGGGAGGC GGAGGTGGGT GGATCACCTG 2400
AGGTGAGGAG TTCGAGACCA GCCTGGCCAA CATGGTGAAA CCCTGTCTCT ACTAAAAATA 2460
CAAAAAATTA ACCGGGCGTG GTGGCGGGCG CCTGTAATCG 2500