EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS076-28179 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr19:11202920-11204720 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr19:11203473-11203485GTTTGTTTGTTT+6.32
SPI1MA0080.4chr19:11204085-11204099TACTTCCTTTTTTT-6.3
SPICMA0687.1chr19:11204085-11204099TACTTCCTTTTTTT-6.79
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_01022chr19:11202909-11203678Adrenal_Gland
SE_01022chr19:11203682-11206319Adrenal_Gland
SE_12085chr19:11199436-11204174CD3
SE_14622chr19:11198676-11207877CD4_Memory_Primary_7pool
SE_17142chr19:11199458-11204099CD4p_CD225int_CD127p_Tmem
SE_19715chr19:11199366-11204828CD4p_CD25-_Il17p_PMAstim_Th17
SE_20994chr19:11198676-11207604CD8_Memory_7pool
SE_22774chr19:11199079-11204103CD8_primiary
SE_23239chr19:11198937-11203807Colon_Crypt_1
SE_23239chr19:11203891-11206070Colon_Crypt_1
SE_24095chr19:11201137-11203799Colon_Crypt_2
SE_24095chr19:11203945-11204272Colon_Crypt_2
SE_24095chr19:11204321-11204812Colon_Crypt_2
SE_24928chr19:11199034-11204236Colon_Crypt_3
SE_24928chr19:11204281-11204823Colon_Crypt_3
SE_26902chr19:11198490-11204883Esophagus
SE_28429chr19:11198835-11207741Fetal_Intestine
SE_29308chr19:11199027-11207595Fetal_Intestine_Large
SE_29905chr19:11198697-11204091Fetal_Muscle
SE_31737chr19:11199668-11204904Gastric
SE_34726chr19:11198191-11208606HeLa
SE_36050chr19:11198460-11204893HMEC
SE_38264chr19:11198668-11208150HUVEC
SE_40068chr19:11198411-11207591K562
SE_42817chr19:11199051-11207805Lung
SE_44493chr19:11198423-11203875NHDF-Ad
SE_44932chr19:11198436-11204000NHLF
SE_44932chr19:11204002-11204881NHLF
SE_47094chr19:11203332-11203713Ovary
SE_47094chr19:11204371-11204735Ovary
SE_47693chr19:11201130-11203607Pancreas
SE_47693chr19:11203842-11204276Pancreas
SE_47693chr19:11204321-11204840Pancreas
SE_49361chr19:11199614-11203237Right_Atrium
SE_49361chr19:11203270-11203861Right_Atrium
SE_49361chr19:11203878-11204812Right_Atrium
SE_50772chr19:11198863-11207767Sigmoid_Colon
SE_52540chr19:11198883-11208401Small_Intestine
SE_54059chr19:11198844-11207806Spleen
SE_57847chr19:11202662-11203691VACO_503
SE_58185chr19:11202917-11203117VACO_9m
SE_64571chr19:11198697-11204072NHEK
SE_64571chr19:11204114-11204825NHEK
SE_65732chr19:11198652-11207882Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191120296311203178
Enhancer Sequence
TTTTGATGTC CCTTTTCCTT CCACACTCTG TCCCAACTGT CAAGCAAATA GCCTTTTGTT 60
GCTAAGAGAC TGCAGATGTA ACCGACCAGC AGCAAACAGT GAGTCAGGCT CTCTCTTCCG 120
GAAGCAAAAT CAATTGCTGA GATCACTCTG GGGAAAATAC CCACCTTATT TGGAAAGAAG 180
CACTGATCAA TTGATGTCTA TTTTTTTTTT TTTTGAGTTG GAGTCTCGCC CTGTCACCCA 240
GGCTGGAGTG CAATGGCATA ATCTCGCCTC ACTGCAATCC CCGCCTCCCG GGTTCCAGCA 300
ATTCTCCTGC CTCAGCCTCC TGAGTAGCTG GAATTATAGG CGCCTGCCAC AACACCCGGC 360
TAATTTTTGT ATTTGTAGTA GAGATGGGGT TTCACCACGT TGGCCAGGCT GGTCTCGAAC 420
TCCTGACCTC GTGATCCACC CGCCTCAGCC TCCCAAAGTC CAAGGATTGC AGGCGTGACC 480
CACTGTGCCA GCCAATCAAT TGATTTCTCA TTCATTTTCA GCTGGCTCTG TTCCCTTAAG 540
CCAGGGGATT TTCGTTTGTT TGTTTCCCCT TCAAGGAAAT GATTCTAGCT ACAGTTTTGA 600
TTTCCTTGTA CAACTGTTTT CAGTAGCACA GGGAAAGAAA ACATCGAAAG CATTCACCAC 660
CTCATTTGTG TGCTGGGGGA AAAAGCAGAA ATGTGTATTC TCTTTTTTTG TTTCGATGAC 720
CTTGTTCCTG ACTTGTTACT CGTGACTTGA GAGATCAGAG GGCTAGAGGA CTAGAATTTA 780
TAGAGGTGTT TTTTTTGTTT GTTTATTTTT GTTCGAGTTG CCCAGGCTGG AGTGCAGTGG 840
CGCAATCTCG GCTCACTGCA ACCTCTGCCT CCCAGGTTCA AGCGATTCTT CGGCCTCAGC 900
CTCCTGAGTA GCTGGAACTA CAGGCGCCCG CCACCACACC CAGCTAATTT TTGTATTTTT 960
CAGTAGAGAT GGGATTTCAC CATATTGGTC AAGCTGGCCT CGAACTCCTG ACCTCGTGAT 1020
CCACCCGCCT CAGTTTCCCA AAGTGCTGGG AGTACAGGCG TGAGCCGCCG TGCCCGGCCT 1080
TTTTGTGTTT TTGTGTTTTT GAGAGGAGCT CATTGCTTTT TAGGCTTCCC TAGCGTGAGA 1140
AAATCTGGGG ATCCATGCTC TAGTTTACTT CCTTTTTTTT TTTTTTTTTG AGATGGAGTC 1200
TCGCTTAGAT TGCCTAATCT CAGCTCATTG CAACTTCTGC CTCCGGGGTT CAAGGGATTC 1260
TCGTGTCTCA GCCTCCTGGG TAGCTAGGAT ACGGGCACCC GCTACCATGC CTGGCTAATT 1320
TTGTACTTTT AGTAGAGACA GGGTTTCGCC ACGTTGGCCA GGCTGGTCTC GAACTCCTGA 1380
CCTCAGGTGA GCCGCCTGCC TTGGCCTCCC AAAGTGCTGA GATTACAGGC GTGAGCCACC 1440
GCGCTTGGCC TAATTTGCTT TTCCTGAAAT TCAAATGGTC TAATATGAAA AACGCCAACC 1500
TTGCTTGAAA GAATAAGAAA GAGGTGCGGT TTCGTTGGGC CGTTGATGTT TGGAACAGGA 1560
CTGGTTTTGT CCCCTTGCTC GGAAAGGGCA GCAACTGTGA GGACAGCTCC CTGACGTGCT 1620
CTCACTCAGC ACTGTTCCGT TCCTGAGCAC TGTCCCCACT AGCTAGGCCA AGGGAGCTCA 1680
TTTGGCAGGC AACTGCTGTC TGGCTGCGCC TGTGGCAGTA AAATCTGCCT TTATTTTTTG 1740
GAGGCAGGGT CTTGCCCTGT CGCTCAGGCT GAAGTGTGCA GTTATAGCTC ACTGCAGCCT 1800