EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS148-00386 
Organism
Homo sapiens 
Tissue/cell
NHLF 
Coordinate
chr1:43405900-43408280 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6657798chr143408279hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr1:43406837-43406851CTGAGTCATTTCCC-6.06
NFE2L1MA0089.2chr1:43407593-43407608GCATGACTCAGCAGG+6.75
Nfe2l2MA0150.2chr1:43407591-43407606GAGCATGACTCAGCA+7.66
ZNF263MA0528.1chr1:43407030-43407051CCCCAACCTTTCCCCTCCTCC-6.09
ZNF263MA0528.1chr1:43408088-43408109CCTTTTCCTCTTCTCTCCTCC-6
Number of super-enhancer constituents: 53             
IDCoordinateTissue/cell
SE_01795chr1:43403674-43411142Aorta
SE_02447chr1:43405569-43410613Astrocytes
SE_04284chr1:43406405-43408666Brain_Anterior_Caudate
SE_05390chr1:43406422-43410832Brain_Cingulate_Gyrus
SE_06192chr1:43406287-43411226Brain_Hippocampus_Middle
SE_07319chr1:43406534-43411143Brain_Hippocampus_Middle_150
SE_08269chr1:43406272-43411134Brain_Inferior_Temporal_Lobe
SE_10377chr1:43406726-43412417CD19_Primary
SE_11009chr1:43387831-43425728CD20
SE_13825chr1:43406488-43407528CD34_Primary_RO01536
SE_14471chr1:43395753-43414527CD4_Memory_Primary_7pool
SE_19657chr1:43406292-43410967CD4p_CD25-_Il17p_PMAstim_Th17
SE_20345chr1:43407577-43412424CD56
SE_20799chr1:43405756-43409955CD8_Memory_7pool
SE_22754chr1:43406075-43412634CD8_primiary
SE_23189chr1:43399749-43406265Colon_Crypt_1
SE_23189chr1:43406366-43410995Colon_Crypt_1
SE_23904chr1:43406747-43407203Colon_Crypt_2
SE_23904chr1:43407223-43410890Colon_Crypt_2
SE_25177chr1:43406652-43411022Colon_Crypt_3
SE_26580chr1:43395721-43413249Esophagus
SE_29267chr1:43400819-43410293Fetal_Intestine_Large
SE_31882chr1:43406451-43411068Gastric
SE_33837chr1:43401475-43412846HCC1954
SE_34353chr1:43395339-43412997HCT-116
SE_35049chr1:43400682-43411164HeLa
SE_36013chr1:43405529-43411011HMEC
SE_37191chr1:43404622-43414101HSMMtube
SE_38794chr1:43405440-43410875HUVEC
SE_39883chr1:43405665-43410931K562
SE_41038chr1:43405665-43414583Left_Ventricle
SE_41620chr1:43406373-43411014LNCaP
SE_42796chr1:43405575-43411121Lung
SE_49782chr1:43406287-43407314Right_Ventricle
SE_49782chr1:43407568-43410944Right_Ventricle
SE_50202chr1:43396219-43406255Sigmoid_Colon
SE_50202chr1:43406339-43411463Sigmoid_Colon
SE_54088chr1:43406450-43408242Spleen
SE_55340chr1:43407386-43410138Thymus
SE_55821chr1:43405505-43410178u87
SE_57045chr1:43405486-43406260VACO_400
SE_57045chr1:43406294-43410932VACO_400
SE_57417chr1:43405825-43410963VACO_503
SE_58269chr1:43406518-43407187VACO_9m
SE_58269chr1:43407361-43407923VACO_9m
SE_58269chr1:43408012-43408449VACO_9m
SE_58561chr1:43388242-43430420Ly1
SE_60624chr1:43388552-43428820DHL6
SE_62392chr1:43388423-43425814Tonsil
SE_64094chr1:43405747-43410036HSMM
SE_64340chr1:43405657-43411071NHEK
SE_67781chr1:43405505-43410178u87
SE_68708chr1:43406265-43410984H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr14340610843407009
chr14340735543407700
Number: 1             
IDChromosomeStartEnd
GH01I042929chr14339554143414526
Enhancer Sequence
CTCTTCACCC AATCGTAGTG AGGCTTCTAT CCACGCTGTG CCACCCAGTC AGCCCGAGTG 60
GCCACAAGGC CACCATCGCC TCTTCTGCAT TCAGCAATGT GGAGAGGCTT GCCCAGTTCA 120
ACCCCTGGGG TACCCGATGG CCTTCCTCCA CTCACTATCC ACCAGTGTCT ATTACTATGA 180
CAGGCACCGT TCTAGGCACT AAGGACACGG CCGTGGACAA ACCAGACAAA TACCCTGGCC 240
CTTCGATGGC TTACATTATC CCTCTGTCTT GGGAGGGTAT CCTCTCCTGG TTTTAGAGAT 300
ACCAGCTCTT GTTCTTCTAC TTAGGGTCTT TTTCTAGCAA TGGGTTGTTC TCTGGGGCCT 360
TGATCTTTTA CTTTTAATTT TTATTTATTT AATTATAAAA TTGAGATGAG GTCTTGATGT 420
GTTGCTCAGG CTGGTCTTGA ACTCCTGGGC TCAAGTGATC CACCCACCTC AGCCTCCCAA 480
AGTGCTGGGA TTACAGCGTG AGCCACATGC CCGGCCTTAA TCTTCATTTC TCTTTTTATT 540
CCACAGTCTC CCTAGAAGAT CTTTCTCCAC TGTGTGGATA CCAGTGACTA ATTCTCAACT 600
TTTCTCCAGC CTGGGTCTAA GAAACAGACC CATACATACA GGTGCCTCCT GCACATCTCC 660
AGCTGTGTCA CCCCACGCCT CCATTCCTGC ACATCCCACG GCCACCTCTC AGCTCCTGGC 720
ACACCTGCTC CTTCTTCAAA CCACACATCA CCCATGCCAG AAACCTAGAA ACCATTTTTA 780
AACCCTTCTC TGTTGCCCTC GCACGGAATT GATGACCAAA TCCTGTCCAT TCTTCCTCTG 840
AGGGTTTGCT TTTATGTCAC TAGTCCAACG GCAACTTTCT TGATGGTTTC CCGTCTCTAG 900
TCTCACATTC TTAAGTCCGC CCCTCCATAC CAGACGCCTG AGTCATTTCC CTACAATGCA 960
AGTCTGATCA CGTCTGCCCT GGGCAGTGGG TCCCTATTGT CCTCATCCTG AAGTCCATGC 1020
TCCCTAGCTG GGCCCCCGTG CTGGTGCCCA TCCGCCCCTT CTGACTGTGC CGTGCCATAC 1080
TCACAAGGCC CTTTGTGGTC TGGCTCTTGC CTACCTTACC TTGTTGACCT CCCCAACCTT 1140
TCCCCTCCTC CTGTTCACTC TAGTGACACA CTAAACTACT CACGCTTTAC TGAATGCCAG 1200
GCTTTCTGTC TTCTGGGCAT TTTGCTTTGA AGGCCCCCTG CTCACCCCAA CCCTGTTCTG 1260
TTTCTGGAAA ACACCTCCTC TGTCCTGGCC TTAGAGTCCT AGTTCTGTCA TTAACTCACT 1320
ATGAGATCAC AGTCAAGACA TCATTAAATC CAGTAGCTGT CAACCTTGGC TGCACATTCG 1380
AATTGGTTGG GAAGCTTTTA ATTGAATGCC CAAACAGCAT CCCAGACCAA TTAAATCAGA 1440
ATCTGGGGGC GTTCTGGAAA CCCCAATGTG CAACCAAGTG GAGAGCTCAA CCTCCCTCTG 1500
TTTCCTCCCA GCCTGTCTTA CAGACTTTCC ATCTGTAAGG ATTCCCAAAG GGAGCCAGTT 1560
CTGAAGCACA CACTTTGGCA AGAGCTGTCA AGAGCACTTA GCAAATGCAG GGCTTGGGGC 1620
TGGTCCAAGC ATGGGCCCAC GGTCTCCATG CCCAGCAAAC TTGGAAAAGT CCTGTCACCT 1680
CCCCTGCAGC TGAGCATGAC TCAGCAGGCC AAGCCTTCCT GGTGACTTGC TCCTCAGCAT 1740
CGGGCGTGGC CCCATAGCCA CTGTCTGCCT ATTTGGAAGA AGCCCAGCTA ACTCTAGACA 1800
CTACCTGGTT CCCCCAAACA GGACCCTGAT CTTTGGGAGT CACTGCACTC ACTTTCTAGC 1860
CCCATCCGTC TGGACAAGAA ATGTGGTCCT GACGTGAGGA CTGCCCACTC TCATTTGGTC 1920
CTCTCTGGGA AGGTACAGAT TTTTAAACGG GCAAGGCAGC TGGTTAGGAA GACAACCTGA 1980
GGCCATGGAA ACAACAGAGC TTGGCTTCTG ACTCCAGCAT TCAATAGCTT TGTGACCTTG 2040
GGCCTGTCGG CCATTTCATC TGCCTGGGCC TCAGTTTCCG GGTCTACAAA ATGGAAATCA 2100
CCACCCAATC TCATAAACAC AAGCAAAATG CCTGGTACAG AGGAAGGGCT CAGTTTCCTT 2160
TCCTGTCCCT GCCTCCTACC CCCTACCCCC TTTTCCTCTT CTCTCCTCCT TAATGCAAGT 2220
AGGCTGGGCT GGAGGAGATG GTCTAGGTCC CTTCCCATCC TGACATTCAA GTAAACAAGT 2280
GAGGACAGAT CTAGGATGCA CGGCAGGGAG GAGGAAGCCA GCACAGACCT TCACCCCCTG 2340
TGGCTCCCTA GGGCAAGACG CCATTTCTGC TTTGACTGCC 2380